Solidaridad de la Unión con Ucrania
Prozorro+: plataforma ucraniana de contratación pública
Unrevised Machine Translation
Romania-Iași: Blood-testing reagents
Section I: Contracting authority
Main address: http://www.sfmaria-iasi.ro
Address of the buyer profile: www.e-licitatie.ro
Section II: Object
Framework Agreement to supply consumable reagents
Framework Agreement to supply consumable reagents — according to the tender specifications.
PAEDIATRIC EMERGENCY CLINICAL HOSPITAL “SF.MARIA” IASI
Trusa for the semi-quantitative determination of calprotecectin in faeces.
Its pack count cases with internal control included, containing paprious cellulose with specific monoclonal antibodies — calprotecectin.
The internal control area and that of its test either for different colours to provide a rapid view and correct for both the internal control of the reagents and the positive result of the test in all working conditions, by daylight or at night.
It shall specify the cut-value and the interpretation of the results on the basis of that value.
The buffer or extract solution in plastic bottles.
Its vial contain stopper for infilling or insurgency, with faeces collection and/or pipettes for the harvesting of liquid seats.
The heading has been used as a painter for the transfer of the painting from that mixture into the work box in order to avoid contamination during work
Test tube 13 * 100 mm, DIN PLASIC DOC
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— either ultrachransptheta, round-bottom,
Dimensions 13 × 100 mm,
Volume of the 7 ml test tube,
— laid down with a lid on behalf of polyethylene,
Up to 7500rot./min by the strength of the centrifugation scale,
— packaging 500buc./punga.
Pomegranate payment of 25x200m sterilisation
Flat sterilisation rolls, (excluding volume) 2 IND 25MMX200M
Pathological level control for haemoglobin haemoglobin level
Control for the pathologic level pathophylogic for Hb A2 electrophoresis, compatible with the laboratory of the laboratory for HYDRAYS 2.
PT CARD. TRUSA ASLO/CRP
Test cards for latx-agglutination,
— whether or not made of board, plasticised,
— present 6-8 circles, individual diameter greater than 1 cm,
White colour cards with non-agra coloured circles.
Reagent kit for determination of FVIII activity: C
The method of detection is photometrica.
— Set 4 sizes for calibration of the four-point reaction, with traceability certificate
Sub-layer FXa + α NAPAP
— Reactive that competes phospholipids with albumin
— Reasset that has fixed, FX, Ca2 +, albumin, thrombin
— imidazole 3.4 g/l
— Tamon tris 6.06 g/l
Trombouler XR analyser compatible reagent
CA as 19-9 Reasset compatible with the Architect analyser
A quantitative dosing assay of CA 19-9 (sandwich test) in serum and human plasma compatible with the 4100 Architect analyser.
Ready to use reagents: microparticles coated with CAPM 19-9 monoclonal antibodies, monoclonmonoclonal antibodies 19 to 9 with acridyl phosphate (conjugate), Diluent solution for the manufacture, solution Pre trigger, Trigger solution, Wash Buffer
Impachia: sealed cartons with the date of manufacture and the date of expiry of those cartons.
Immunobut kit for allergens in milk and gluten
The panel should allow the concurrent analysis of the following parameters in accordance with the current quality standards: F02 Milk, f76 Alpha-Lactalbumin, f77 Beta-Lactoglobulin, f78 casein, e204 Albumine Serica bovina, f79 Gluten.
The panel shall have a nitrocellulose membrane, determined, impregnated with allergens and 5 standardised calibrators according to 1st WHO 67/86 for human IgE for individual calibration
The panel shall use an immunoenzyme principle with a nitrogen membrane support (immunoblot).
The truffle of reagents must include components such as: antibody reagent, conjugated reagent, substrate reagent, Wash solution reagent in the liquidation, not freeze-dried, ready for use.
Its tests may be carried out by serum or plasma and the maximum volume of the sample should be 300 μl.
Incubation times must not exceed 3 hours.
The paediatric panel shall allow the holds in a refrigerator for 7 days and for those stored in -20. oC specify the period of stability.
The stability of the reconstituted solution of inhibition should be at least 2 weeks.
The processing of the cheese must be automatically carried out using the equipment of the laboratory.
The software for the interpretation of the results must be in Romanian. it generates a report from the Romanian language analysis and connected to the Laboratory Information System, with the possibility of producing a history of patient results
The Supplier must provide internal quality control for testing the correct functionality of the scanner used in interpreting the results.
Its results are either expressed in and automatically classified in 6 classes of allergies according to the classification of EACs.
Anti CPC — Resolute actively compatible with the Architect analyser
Quantitative dosing test for Ac anti PCC, in serum and human plasma, compatible with the CI4100 Architect analyser.
Ready to use reagents: microparticles coated with anti sera CPC, and anti polyclonal CCP/marc with acridinium buffer in ESM buffer, Trigger, pre- Trigger
Sensitivity > 99 %
Specific character > 99 %
Reagents package compatible with automatic ELISA.
A Ac. Anti Gliadina deamideata IgA (quantitative method Elisa)
B Ac. Anti Gliadina degamata IgG (quantitative Elisa method)
Amount of Ac anti -Sacaromes cerevisiae IgA — quantitative ELISA
Red Ac anti -Sacspicices cerevisiae IgG — quantitative ELISA
E Calprotecectin -quantity of faeces ELISA
F Ellastaza pancreatic ELISA method
Giant anti Helicobacter pylori IgG (quantitative method) ELISA
Anti toxoplasma gondii IgM (qualitative) ELISA
I Anti-corps VEB IGM (VIRUS EPS BARR) METODA quantitative ELISA
J Antibodies anti VEB IGG (VIRUS EPS BARR) METODA quantitative ELISA
K Antigen HBs (qualitative method) ELISA
L Ac.anti CMV IgM (qualitative method) ELISA
M Ac.anti CMV IgG (quantitative method) ELISA
Anitoxenoplasma gondii IgG (quantitative method) ELISA
O Ag/Ac HBE qualitative ELISA
P ANA screen TOTAL (-ds DNA, HISTNE, SS-A (Ro), SS-B (La), Sm, snRNP/Sm, Scl-70, PM-Scl, Jo-1, centromeric antigen) the qualitative ELISA method
R Anticulti — myeloperidase — (p-ANCA) quantitative ELISA method
Lis Mycoplasma pneumoniae IgA-quantitative ELISA
T Mycoplasma pneumoniae IgG-method quantitative ELISA
Mycoplasma pneumoniae IgM-Method the quantitative ELISA method
Placenta FOOD STAMP RODAC for microbiological control of working areas for the determination of total number of sprouts
Used for the detection and designation of micro-organisms on areas of the sanitary importance for assessing the extent of their contamination (control of the area infection). Their structure ensures full contact between the agar and the area to be controlled. Contact area of each placer: 10 cm². Medium of the readily moulded unmoulded culture which is sterile with the internal diameter of 50 mm on which it is printed: the name of the medium; date of minimum durability; number of lottion.Packaging in labelled boxes on which it is specified: the name of the medium, the way of preserving the environment and the conditions of transport and storage. Contents of boxes: plastic bags with 5 placenta. Validity: minimum 90 days after delivery
Methylene blue solution 1 %
Multiple colour in bacteriology
Count 1 % minimum methylene blue
Packing: plastic bottles of 1 000 ml on which the components, shelf life, transport and storage conditions are specified. Used for staining of the microscopic preparations
Merck’s indicator of pH type
Universal strip for all media analysis, pH range = 0-14, size 6x85 mm, 100 tests/case; its colour sites shall not enter any of its colours.
AG Cryptosporidium and Giardia
Quality determination of Cryptosporidium/Gigardia antigen in faeces.
Its pack count separate boxes with casings containing coated cellulose with Cryptosporidium and Anti- Giardia.
The test shall be used for the detection of Cryptosporidium parvum and Giardia lamblia in human faeces.
Its internal control box included.
Cross the reactivity with other bacterial species.
Its vial contain the inthreaded or insurgent stopper with the faecal material collection device. And/or pipettes for the harvesting of liquid seats.
It is also used as a painter for the transfer of the painting from that mixture into the work box to avoid contamination during work.
Cost determination of the antigen of Campylobacter in faeces.
Its pack count cassettes with coated nitrocellulose membranes with monoclonal antibodies to Campylobacter.
Its vial count the plug of the insurgency, or inthreaded, with the faecal material collection system and/or pipettes for the harvesting of liquid seats.
Reference strains of Haemophilus influenzae ATCC 10211
The reference strain used for quality internal control of the media of the culture/biography/identification of micro-organisms. Lyophilisata microbial culture, exclusively from the first generatie (first passage) of the master cultures of micro-organisms resulting from international recognised culture collectors (ATCC/NCGC)
Does not require freezing to -70 deg C
Tabulation of each of 106 to 109 microorganisms in the form of discs or microtablets
Packing in bottles with 10 to 12 discs, labelled with it: the name of the reference mark, the method of preservation and the conditions of transport and storage.
The validity of the stems: 9-12 months after the opening of the bottle
Can Grunwald type Merck
Solution for the staining of peripheral pressure smears and maduva, which contains the modified elution solution for microscopy.
Packed in a 500 ml plastic bottle.
Running conditions at 15-25 ⁰ C
Solution to the IVD certificates
EHEC VT1 + VT2
Truffle — rapid tests for qualitative simultaneous determination of verotoxins 1 and 2 faecal material of E.coli
Immunochromatographic working method — rapid tests
Box 2 (VT1) separated from the (VT1) and verotoxin 2 (VT2) cuvées to avoid interfering in the reading of the result
— a buffer or extraction solution in plastic bottles
— its vial contain the stopper, or the inthreaded lid, or the insurgency with the faecal material collection and/or pipettes for the harvesting of liquid seats
— the stopper or its lid is also used as a painter for the transfer of the product into the working box
Box aiba to quality internal control lane including stripper
— In the internal control area and that of the Teast either of different colours to ensure the rapid view of the correct between the internal control of the reagents and the positive result of the test in all working conditions, either by daylight or at night
— SA produces instructions for working in Romanian
— Its specifically limits the limits and inconsistencies that can be caught as to the result
— A period of validity of at least 6 s months
The result was obtained within 10 minutes of the lodging of the cassette-type
— its sensitivity and specificity test > = 98 %
Precipitation kit for ciclosporin compatible with Archect analyser
Reagent kit consisting of:
—1 fl of solubilisation reagent for ciclosporin
—1 pl of precipitation reagent for ciclosporin
Loffler blue methylene blue Loffler
For simple colouring in bacteriology
— 300 ml saturation methylene blue solution
— KOH water solution of 0.01 % 1 000 ml
Reference strains Salmonella typhimurium ATCC 14028
Rock rock, sterile, of good quality, without blood clots, having a minimum shelf life of 1 month (achieving quality during this interval)
Mycobacterium tuberculosis — quantitative ELISA method
1.TRussian ELISA with a minimum of 96 tests with standard well ELISA plates with well plates
2 To be used in working mode as biological serum or human plasma
3.its test is based on indifferent technology for the detection of infections with Mycobacterium tuberculosis
4.The test determined IFN -gamma rays from total blood cells to identify, associated with the infection with Mycobacterium tuberculosis specific antigens
5.Its Kite includes special collection tubes that are fully coated with negative, positive and antigen controls
6.Senability and specificity of its pack shall be at least 95 %
7HH the programme for reading and interpretation of the results obtained
8.In the package leaflet the type of the calibration curve that is used by the manufacturer of that kit shall be specified.
CA 125- Reasset compatible with the Architect
A quantitative sandwich dosing test for CA 125 (sandwich test), in serum and human plasma, compatible with the 4100 Architect analyser.
Ready to use reagents: microparticles coated with the monoclonal antibodies anti CA 125, monoclonal antibodies anti CA 125 marker with acridinium phosphate (conjugate), Diluent for manual dilution, Pre Trigger, Trigger, Wash Buffer
STERILE SEIZED GRADED 1
Bacteriologic experimental use for inoculation,
Placed in a 1μl calibration enclosed with the appropriate μl loop
Used in microbiology laboratories for the procurement and inclusion of culture media,
To be sterile, flexible,
The material from which the inoculation loops are made are deformation resistant, so as to enable the volume taken over to be processed safely,
Packed in 20 bucati packs,
The plastic put up either in a transparent plastic bag with the zip or on its packaging, or with one of the plastic and one of the plastic film, the transparency, glued to the distance concerned in the proceedings of the mills after the opening of the package.
Reagent band for determination of FVIII inhibitors
It must contain:
Plasa lyophilata with a standardised content in FVIII,
Lyophilata with the present inhibitor FVIII and determined value,
Plasa lyophilata without this FVII inhibitors,
— sterile suture materials
Recomolyser XR analyser compatible reagent.
Reagent kit for the determination of the activity of the C protein, consisting of:
Drivers of C protein (Sardinian vein extract)
— Poor’s deficiency in Proteina C,
DimethylHBs compatible with the Archect analyser
Match specific for the AcHBs for Architect c1000 analyser
Sterile Pasteur pipettes of sole use, made of plastic sheeting, packaged individually in paper, plastic or plastic/paper or plastic (one in front of the plastic and one in plastic).
Its packaging must be bonded to the small distance of one of the ends to allow for the disposal of the ussoara.
Patient identity cards for the patient’s bed (patient and unit of transworn)
The AB0 test card and the test AB0 + D test are used for the direct verification of identity immediately prior to blood transfusion (bed test). The test shall confirm the characteristics of the ABO or ABO and D of the patient whose characteristics have been determined in advance and shall ensure the compatibility of the blood group of the recipient with the village to be passed through.
This could lead to possible detection of errors.
The test may also be carried out in the case of erythrocyte concentrate.
Principle of the test
Test cards impregnated with dried specific monoclonal agents.
Test principle: haemagglutination test for the purpose of determining those erythrocyte inhibitors.
The blood groups of the AB0 system, i.e. the factor D of the Rhesus system, are defined by the presence or absence of antigens A, B, and D in red cells.
If these antigens are present in red cells, they will agglutinate by suitable antibodies (positive reaction).
It can be used for identity tests AB0 and AB0 + D of recipients and donors/blood bags (double card) and for testing two recipients (the simple card).
Card AB0 + D:
The double card containing four surface of the reaction surfaces: one with anti-A (clone A003, 1: 32) 200 IU/ml), one with anti-D anti-D (clone BS226, titre: 200 IU/ml), one with anti-B (clone B005), and a surface for the test blood and for own-check blood respectively. 0.1 % NaN3.Stabiliser: one for the recipient and one for the donor.
Antibodies are derived from cultures of stable cell lines and show the specificity and reproducibility of monoclonal antibodies.
Cards packaged under film and stored under appropriate conditions may be used until the shelf life of the sheet and the outside label have expired.
The card must be removed from the sheet only on
A collection of reagents used to determine the level of AT III by the automatic analyser cromoliger XR constant from:
Trombina lyophilata 43 IU/bottle,
— Cromogen sublayer
G/l Tampon Tris 3.03 g/l
AG Helicobacter pylori
Clinical determination of the Helicobacter pylori antigen in faeces.
Its pack count cases with casings of nitrocellulose with monoclonal antibodies to Helicobacter pylori.
Its truffle by limits, interfering with the interpretation of patient outcomes as well as crossreactivity with other bacterial species.
Kit for the determination of electrophoresis of haemoglobin
Kit for electrophoresis acrylamide compatible haemoglobin with analyser HYDRAYS 2 Sebia; to identify it by the migration method to the agarose gel at alkaline pH that would allow the separation and quantification of normal blood haemoglobin (HAD, Hbf, HbA2) and the separation of the main blood haemophilia of medical interest (HBS, HBD, HBC and HBE) as well as the separation of normal haemoglobin levels of the newly born (Hbf and HBA) and pathological points (S, C,E, D,Bart); to allow the clear separation of fractions with the possibility to detect other pathological findings of Hb.
Sample of his/her reagents count low number of samples/gel (e.g.: 7 samples/gel), its 10 gels/kit, a dedicated solution for haemolysis, filter paper, buffer strips, single use applications, staining solution, Dilution solution for the staining solution;
PARASITOLOGIC EXAMINATION (NON-STERILE)
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The volume of the vessel is 15 to 20 ml, 20 mm diameter and 60 mm in diameter,
The body of the container is either very well glued to the bottom of the body so as not to allow the preparation of solutions
The body of its container with a system of infileing ethanes, which is to be preferred on the outside,
There is a cap on its cover for harvesting and thread, which is to be quoted on the inside,
The spoon for harvesting it is either closest to the base of the vessel,
Packaging in plastic bags of 500 to 100pieces.
SURAT FUCS-ROSENTHAL, HAVING ITS SOLE USE
— 10 llates of Fucs — Rosenthal, of the single
Use, intended for the number of leukocytes in urine
Of ultronransparent plastic,
Each room had a grid of 81 small patents,
Each small patat has a volume of 0.1μ and the area of 0.111 mm2,
— packaging 100buc./cutie.
Pomegranate payment of 10x200m sterilisation
Rola sterilisation payment, (excluding volume) 2 IND 10MMX200M
Pomegranate payment of 40x200m sterilisation
Flat sterilisation rolls, (excluding volume) 2 IND 40MMX200M
Detectable set antibody kit with 3 red blood cells
Form of presentation and characteristics:
Set of three red assays for agglutination in the gel column, via Test Coombs Indirectly or Test salin, phenotypated for major antigenic systems, Rhesus, Kell, Kidd, Duffy, MNSS, Lutheran, Lewis, P1 and Xga.
The Rhea-type phenotype will be different for each red blood, but mandatory in one of the following formulae: R1R1, R2R, rr.
All packages will be blood group O, suspended at 0.8 %, with LISS and stabilising solutions.
The erythrocytype phenotype is marked in the antigen map of the consignment delivered (identical to the parlamented screening set).
The assay kit will have a conditioning condition of no more than 200 tests.
Stability of 7 weeks after the date of manufacture; at delivery the set shall be at least 6 weekly shelf life.
Used for detecting antibodies regulin in the Coombs Indirecte or saline test, with agglutination in the gel column, in cards compatible with the equipment in the form of the release system for immunological determinations.
The original instructions for use of the producer, accompanied by the translation of the Romanian translation and the quality certificate of a production batch will be presented. A certificate of the compatibility of the reagent with the system of the endowment of the unit.
Measurement unit/Packaging: Measurement unit: 1 kit, Packaging: 1 box x 3 vials x 10 ml.
• Certificate from the producer of the reagents demonstrating the compatibility of the reagents with the equipment in carrying out the equipment
Sworn statement (original in pdf)
• Lot of the product by certificate of analysis from the producers certifying their quality
• The use of its reagents does not require recalibration of the appliance or any other intervention and/or additional adjustments
• On the label of the packaging
Nec (Combo Combo 57)
Identification and anocgram identification panel (breakage method) intended for urine isolates compatible with MICROSCAN.
Panel that holds the MIC for: amikacin; amoxicillin; amoxicillin + clavulanic acid; cefeim; ceomum; cefazolin; ceftazidim, cafotaxim; cefoxitin; Cefuroxim; Cefotaxe + clavulanic acid; ceftazidim + clavulanic acid; ciprofloxacin; colistin; Ertapenem; phosphomomycin; gentamicin; Imipenem; mecilinam; nalidixic acid nitrofurantoin; norfloxacin; ofloxacin; piperacillin + tazobactam; tetracyclna, ticarcilina, ticarcilina + clavulanic acid; Tigecycline; trimethoprim/sulfamethoxazole; tobramycin;
REAGENTS PACKAGE FOR THE ANALYSER OF THE AIF 8000
A Troponine I
B double test: NT-proPB/cTnI
C triple test: CKB-MB/cTnI/Myo
E PCT (procalcitonina)
F CysC (Cisatina C)
G Test PT
H Test APTT
Integrator class 4
Strp integrator chemically class 4 for the interior. Each indicator is marked: batch number, date of manufacture and expiry date, class according to ISO 11140-1
CHEMICAL INDICATOR STERILISATION AUTOCALAV STRIP INTEGRATOR 5
Chemical integrator (Class 5) ABUR — strip
Strip rolled sterilisation for sterilisation at autoclave 134oC -7 min/121oC-20 min monitoring all critical parameters: time, temperature, absence of air and quality of steam. Monitor all vapour sterilisation cycles (121oC-134oAnd all the parameters of the cycle. The product shall investigate the possible deficiencies in the operation.
Each indicator is marked: batch number, date of manufacture and expiry date, class according to ISO 11140-1
Gel solution for agglutination in gel column (modified for micro method)
Form of presentation and characteristics: Solution with the modified Ionica PISS (LISS), for the technique of agglutination in the gel column with type cards, which are compatible with the equipment contained in Diamed ID System for immunohaematological determinations.
Use: Used to dilute the standardisation of the test cells used to determine the blood group, the Rhetop phenotype, the Tome Coombs Direct and Transfusion compatibility by Test Coombs Indirectly.
Principle of the working technique: Letter Ionica joasa, showing the rate of the combination of such antibodies to antigen and antibody, agglutination of the cells in the gel column containing the test reagent being recorded as a result of a standardised centrifugal centre.
• On the label of the packaging of the reagents to be provided, it should be noted that:
A. name of the reagent
B. the number of the manufacturing batch
C. volume of reagents
D. expiry date
E. storage conditions
F. name and address of the producer
• its products produce certificates demonstrating that the International ISO 9001, EN ISO 13485 standards are met.
• the Romanian distributor of the system and the reagents (boxes) to prove the proof of the ISO 9001 standard quality system: 2008, ISO 13485: 2012, ISO 14001: 2005,
Reference strains of Haemophilus influenzae ATCC 49144
Used for the detection and designation of micro-organisms on areas of the sanitary importance for assessing the extent of their contamination (control of the area infection). Their structure ensures full contact between the agar and the area to be controlled. Contact area of each placer: 10 cm². Average of the selective and differentiated ready cast in sterile sheets with the internal diameter of 50 mm on which it is marked: the name of the medium; date of minimum durability; the lot number. Packing in labelled boxes on which it is specified: the name of the medium, the way of preserving the environment and the conditions of transport and storage. Contents of boxes: plastic bags with a maximum of 5 plywood. Validity: minimum 90 days after delivery
Control level normal for eklectopheresis haemoglobin
Control for the normal Hb A2 gel electrophoresis compatible with the laboratory of the laboratory for Hb A2.
Control for pathological haemoglories
Control for blood fractures A, F,C, Scompatible analyser HYDRAYS 2 to the laboratory of the laboratory.
Pomegranate payment of 20x200m sterilisation
Flat sterilisation rolls, (excluding volume) 2 IND 20MMX200M
Rola payment sterilisation, 5-5.5x200m
Flat sterilisation, (excluding volume) 2 IND 5-5.5mmx200m
Bowe Dick package 200 autoclave; the middle of the amber pack test to confirm the uniformity of steam penetration
Authorisation kit to detect autoimmune diseases, ANA 14 Profile
Immuno-blotting kit with fixed grooves, with a single casing, to avoid interpretation of possible background effects. An autoimmune profile ANA, which accounts for at least the following parameters, which can be quantified, simultaneously for one patient: EN/SSA-A 52, Jo-1, Sm, CENP-B, La/SSB, History, PM/SCL 100, Rib. Phosphope. PO, dsDNA, Scl-70, U1-snRNP, Ro/SS-A 60, Mi-2, Ku.its function as worked from serum or plasma; processing of its plasma either automata, using the BeeBlot Polycheck equipment from the laboratory of the laboratory.
Placenta FOOD STAMP RODAC for microbiological control of working areas for the determination of this S. aureus
FOOD FOOD STAMP RODAC for microbiological control of working areas for the determination of this coliform
Giemsa type MERCK
Solution for the staining of peripheral pressure smears and maduva
Thermo-sensitivity at 110 mm
A 110 mm wide thermal window
Carbapenem-resistant Enterobacteriaceae (CRE) resistant Enterobacteriaceae (CRE)
Ready-to-use/clean carbapenem-resistant Enterobacteriaceae: E. coli, Klebsiella, Enterobacter, Serratia and Citacrobacter (KESC Group), directly from clinical evidence in 18-24 ore.Formula grams/litre:
Titanium oxide 5.1
Chromogen 1.0 mixture
Mixture of antibiotics 19.0 ml
Agar 15.0.The internal quality control is performed with reference strains: Klebsiella pneumoniae Regulations 13443 and Acinetobacter baumannii NCTC 13420.
Presentation 10 plates packed in foil. A minimum of 6 weeks of validity at the date of manufacture
Anti CPC CONTROL — compatible with the Armchect analyser
Control serum for the detectia of PCC and its ready to use Architect CI4100 analyser
Method of detection used: CMIA
Reference strains Candida albicans ATCC 66027
Packing in flasks with 10-12 discs or answabs/swabs with 2 to 5 labelled packs on which they are labelled: the name of the reference mark, the method of preservation and the conditions of transport and storage.
The validity of the stems: 9-12 months after the opening of the bottle.
Pomegranate payment of 30x200m sterilisation
Flat sterilisation rolls, (excluding volume) 2 IND 30MMX200M
Oil jelly at high temperature for the lining of the autoclave
Anti levelling CCP — compatible with the Armchect analyser
Calibration serum for the detectia of PCC analyser Armchect CI4100
MICROSCOPE SLIDES 20X20
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— dimensiuni:20mm x 20 mm, thickness 0.15 mm,
— packaging 100buc./box, 1000buc./cutie.
CA as 19-9 Archect-compatible calibrator
Calibration serum for AC 19-9 compatible with the integrated Archect CI4100 integrated system
Deficit plasma in factor VIII
Necessary for the determination of the activity of FVIII: C by the one-stage method using the APTT test
The plasma is either freeze-dried with FVIII content below 1 %.
Set of three test papers for agglutination in the gel column by enzymatic Test, phenotype for major antigenic systems, Rhesus, Kell, Kidd, Duffy, MNSS, Lutheran, Lewis, P1 and Xga.
All the packages will be blood group O, papaised, in a suspension of 0.8 %, in the stabilising solution.
The erythrocytype phenotype is marked in the antigen map of the batch delivered (identical to the red blood sample kit for the LISS).
Used for detecting antibodies in the enzyme test, using the technique of agglutination in the gel column, in cards compatible with the equipment on the equipment, Dised System for immunological determinations.
• On the label of the packaging of reagents which
Plywood Agar Chocolate with Vitox type
Ready-to-use plywood with nutritious medium used for the isolation and growth of tedious micro-organisms.
Peptone species 15.0
Maize starch 1.0
Dihydrogen phosphate by K1.0
Vitamin B1 0.0002 L-Glutatamine 0.2
P-amino benzoic acid 0.00026
Nad (Coenzyme 1) 0.005
Nitrate Ferric 0.0004 Thiamine 0.00006 cysteine 0.518
Its quality internal control shall be conducted with reference strains:
Haemophilus influenzae ATCC 10211
Neisseria gonorrhoeae ATCC 49226
Staphylococcus epidermal ATCC 12228
Presentation 10 plates packed in foil.
The date of validity of 14 weeks after the date of manufacture. Storage at 6-12o C. Colour of light brown medium, transparent.
Monovalent O3 agglutination serum — Yersinia enterocolitica
Monovalent O3 serum to identify the serlogica of the Yersinia enterocolitica strains by the agglutination method. Glass/plastic vial labelled with the name of the product and the producer, the shelf life and the conditions of transport and storage.
STERILE ENVELOPED STERILE 10
Placed in a 10μl calibration enclosed with the appropriate μl loop.
12 ML STERILA PLASTIC TUBE
Of plastic, of polypropylene type,
— either ultrachransptheta, round-bottom
Or provided with anethins, on the outside,
With screw cap,
The volume of the test tube is either between 10 and 12 ml,
Inside diameter of either 14 to 17 mm tubes,
The tubes may be packaged individually,
— Packaging 500buc./cutie (punga).
ROLA THARTIE TERMOSENSILBILA 57 MM
Superior good quality paper,
Of monochrome, alba, unpersonalisata,
With a width of 57 mm.
Universal harvesting for the collection, transport and storage of urine, signifies,
Of plastic type polypropylene, ultrachranspaconte,
The body of its container with an external, ethic infilleting system,
A cover made from non-different density polyethylene with thread on the inside,
The volume of the vessel is 60 ml,
Sterile, packaged individually, 500buc./punga.
SELF-ADHESIVE HEAT LABELS
Labels used for printing bar codes using heat head printers,
— compatible with zebra printers,
Of hartie alba, with a semi-hard and a glue.
Pomegranate payment of 15x200m sterilisation
Flat sterilisation rolls, (excluding volume) 2 IND 15MMX200M
Sterile plastic, solely used, individually packed in paper or plastic/paper (one in front of the plastic and one in plastic).
Length 70-120 mm
As 125 NACE-compatible analyser
CA calibration serum 125 compatible
With the integrated Archect CI4100 system
SUMAR tube urine 16 * 100 mm
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Dimensions 16 × 100 mm,
Volume of the 10 ml test tube,
Resistance to centrifugation,
MICRO-SPOCOP76 * 26 * 1 mm, matp to an capat
From the docranspareta bottle,
Dimensions: 76 mm x26mm x1mm,
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— packaging: 50buc./cutie.
Pack — rapid tests for the simultaneous quality determination of Clostridium difficile — GDH, toxin A and B toxin in faeces
Box showing 3 strips with separated pack of nitrofurans with GDH, the A toxin and the B toxin to avoid interfering in the reading of the result
— its vial count the stopper, or the inthreaded lid or insurgency with the device of
Collection from faeces and/or pipettes for the harvesting of liquid seats
— the stopper or its lid is used and as the picurator for the transfer of the product
In the working box
— his or her kit either separate vials containing separate internal control of known quality, used to validate the results
— the internal control area and that of the West of the West either differ in colour to ensure the rapid view between the internal control of the reagents and the positive result of the test in all working conditions, whether by daylight or at night.
The result is obtained within 10 minutes of the lodging of the cassette-type
Section III: Legal, economic, financial and technical information
Tenderers, third parties and subcontractors must not be subject to the conditions laid down in Article 164, 165, 167 of Law No 98/2016. How to meet the requirements of the requirement: all economic operators participating in the award procedure, with the information related to their situation, shall be completed by all economic operators participating in the award procedure.
The supporting documents proving that those assumed by completing the DUAE are expected to be presented, at the request of the contracting authority under Article 196 of Law No 98/2016, only by the tenderers ranked in the first 5 posts in the intermediate ranking drawn up at the end of the evaluation of the tenders.
These documents are i:
1 Certificates of absence of outstanding debts with regard to the payment of taxes, charges or contributions to the consolidated general budget (local budget, state budget, etc.) at the time of submission;
2 The criminal record of the economic operator and of the members of the administrative, management or supervisory body of that economic operator, or of those with powers of representation, decision or control therein, as derived from the certificate issued by the NTRO/constituent act;
3 A declaration on compliance with Article 58 of Law No 98/2016.
If the tenderer falls within any of the situations referred to in Article 58 of Law No 98/2016, his tender will be rejected as unacceptable.
The persons depending on the decision in the CA as regards the organisation, operation and finalisation of the procedure are:
1 Corneliu Mihai Manager
2 Alina Maria Vrabies Financial Director
3 Dogu Alina Nicoleta Sef Service Public Procurement,
4 Ird Alina Mihaela Economist Public Procurement Service
5 Pinzaru Lacraioara Inginer The Public Procurement Service
6 Irina Referent Service Public Procurement Service
7 Nistor Cristina Ioana Under the Public Procurement Service
8 Foache Mihaela Under the Public Procurement Service
9 DRAGOMRESCU Cezarina Doctor- Sef Laboratory Medical Analysis as President of the Commission
10 Morariu Medical assistant Head of Technology Assessment
11 Panzaru Carmen ValValentina Medic Laboratory Mayor
12 Technician — Liliana biologist, technique member
13 Cyubtaru Maria Colrina Bioengineer, Technical Assessment
14 Maxim Irina Medic Primary Laboratory Evaluation Member
15 Janoaboi Elena Chiomost Medical Main — Technical Assessment
16 Belu Alina Bioing. Medical and technical evaluation Member
17 Paiu Corneliu Sef sectie ATI, President of the Evaluation Committee
18 Ivan member of the evaluation committee
19 Lidia LOERIU Member, Transfeuii Point Evaluation Committee
20 Artin Gianina Presearechairman of the Technical Assessment
21 Macovei Paula member of the Evaluation Committee
22 Jigolea Mihaela The Evaluation Committee
1.The economic operators submitting the tender must prove a registered form of registration under the law of the country of residence, to the extent that the economic operator is legally established, as it was not in any of the cases for annulment of the formation, and the fact that it has the professional capacity to perform the activities which are the subject of the contract. The participation of the economic operators participating in the award procedure with the information related to their situation will be completed by the economic operators participating.
The supporting documents proving that those undertaken by completing the DUAE, namely the certificate issued by the NTRO, indicate the subject matter of the economic operator’s activity or, in the case of foreign tenderers, equivalent documents issued in the country of residence. The subject of the contract must be corresponding to the CAEN code of the certificate issued by the NTRO. The original or a true copy of the original will be presented.
These documents are to be submitted, at the request of the contracting authority, only by the tenderers ranked in detail on... www.e-licitatie.ro
Lots shall not: 1,10,11,12,13,14,15,16,17,18,19,2,20,21,22,23,24,25,26,27,28,29,3,30,31,32,33,34,35,36,37,38,39,4,40,41,42,43,44,45,46,47,48,49,5,50,51,52,53,54,55,56,57,58,59,6,60,61,62,63,64,65,66,67,68,69,7,70,71,72,73,74,75,76,77,8,9 For procurement contracts for goods: execution of deliverables of the type specified list of main deliverables of similar products over the last 3 years
Supplement DUAE pt. c
Section IV: Procedure
Section VI: Complementary information
Internet address: www.cnsc.ro