Procurement Summary
Country : Macedonia
Summary : Elisa Kits for the Determination of Antimicrobial Substances in Food
Deadline : 07 Mar 2024
Other Information
Notice Type : Tender
TOT Ref.No.: 98201706
Document Ref. No. : 02152/2024
Competition : ICB
Financier : Self Financed
Purchaser Ownership : Public
Tender Value : Refer Document
Purchaser's Detail
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Given in the technical specification, a quantitative ELISA test kit for the determination of residues of nitroimidazoles (to detect at least dimetridazole, metronidazole and ronidazole), with a detection limit ≤ 1 ng/g for eggs and muscle. The whale must be validated by the producer at least for muscle and eggsQuantitative ELISA test kit for the determination of chloramphenicol residues, with a detection limit ≤ 0.1 ng/g for milk, muscle, eggs, honey, water, urine. The kit must be validated by the manufacturer at least for milk, muscle, eggs, honey, water, urine, Quantitative ELISA test kit for determinationof AOZ residues, with a detection limit ≤1 ng/g at least for tissues, muscle, eggs, honey. The kit must be validated by the manufacturer at least for tissues, muscle, eggs, honey, Quantitative ELISA test kit for the determination of AMOZ residues, with a detection limit ≤1 ng/g at least for tissues, muscle, eggs, honey. The kit must be validated by the manufacturer at least for tissues, muscle, eggs, honey, Quantitative ELISA test kit for the determination of AHD residues, with a detection limit ≤1 ng/g. The whale must be validated by the producer at least for tissues, muscle, eggs, honey, Quantitiesven ELISA test kit for determination of SEM residues, with detection limit ≤1 ng/g. The kit must be validated by the manufacturer at least for tissues, muscle, eggs, honey, Quantitative ELISA test kit for the determination of avermectin residues (at least ivermectin, doramectin, abamectin), with sheetdetection limit ≤ 5 ng/mL. The kit must be validated by the manufacturer at least for liver, muscle, milk., Quantitative ELISA test kit for the determination of residues of fluoroquinolones (at least enrofloxacin, ciprofloxacin, marbofloxacin), with a detection limit ≤ 10 ng/g at least for milk, kidney and muscle. The kit must be validated by the manufacturer at least for milk, kidney and muscle, Quantitative ELISA test kit for the determination of residues of total sulfonamides, with a detection limit ≤ 10 ng/g at least for milk, tissues, eggs, honey. Cross-reactivity least for sulfadiasein, sulfadioxin, sulfamethoxazole, sulfisoxazole, sulfachlorpyridazine to be ≤ 60 %. The kit must be validated by the manufacturer at least for milk, tissues, eggs and honey. Quantitative ELISA test kit for the determination of tranquilizer residues. Cross-reactivity least for promazine, acepromasein, chlorpromazine and limit of detection ≤ 5 ng/g. Kit to be validated by manufacturer at least for kidney and liver, Diffusion test for detection of antibiotics in raw milk with ability to detect concentration of penicillin G greater than 2.0 ppb, Qualitative screening test for detection of antimicrobial substances, at least in animal tissues, eggs, fish at least for β-lactams, Cephalosporines, Macrolides, Tetracyclines, Sulphonamides, Aminoglycosides, Quinolones, Amphenicoles and Polypeptides, Premi test or equivalent. The principle of the test to be inhibition of Baci growthllus stearothermophilus. The test must have validation from a reference laboratory that it has the ability to detect antimicrobial substances at the maximum allowed level or less according to COMMISSION REGULATION (EU) No 37/2010,
CPV Descriptions: Medical equipment, pharmaceuticals and personal care products
Documents
Tender Notice
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