Bids Are Invited For Acquisition Of Hospital Medical Material (Test, Tube, Solution Etc), To Compose The Price Registration System.

Test, Dosage, Chromatographic Beta For Rapid Qualitative Determination Of Human Chorionic Gonadotropin Using Reaction Strips Or Soap, Containing A Combination Of Monoclonal And Polyclonal Anti-Bodies Capable Of Selectively Identifying The Beta Hcg Subunits In Urine And/Or Serum Samples, Sensitivity Up To 25 Very/Ml, Containing All Reagents, All The Reagents, Components, Accessories And Supplements Needed To Perform The Technique And/Or Test. Embarrassing With Product Identification In Portuguese, Procedure, Manufacturer Brand, Date Of Manufacture, Validity And Registration In The Health Ministry. Endoscopes, Neutral Ph, Non -Irritating, Packaging: Spray No, At Least 500Ml, Repaying As Usual From The Manufacturer. The Product Must Be In Accordance With Current Legislation. It Should Be Presented To Present Dermal And Eye Irritability, Bottle, Laboratory Use, For Secretion, Polypropylene, Disposable, With Hermetic Occlusion, Two -Way Jam, Rigid, Graded, 40Ml Capacity. Individual Inbirth, With Product Identification And Brand Identification Data., Tube, For Blood Collection, The Vacuum, In Transparent Polyethylene Plastic, Sterile, With Separator Gel, Without Anticoagulant, For The Obtaining Of Serum, 5 Ml Aspiration Volume, Rubber. Siliconized, With Protective Plastic Lid, 13 X 100 Mm Dimension. Embeddown With Product Identification Data In Portuguese, Batch, To Be Born, In Polyethylene Plastic, Not Sterile, With Edta K2 Or K3 Anticoagulant, With A Capacity Of 400 To 500 Blood Microlyters, With A Pipe Co -Capulated Beead Or Accompanied By Funnel, Protective Cover In Color Standardized, On The Label Of The Primary Packaging Or Tube Should Be Contained In The Additive Or Description Of The Content, Nominal Volume And Fill Line. Packaging: Primary Packaging Packed According To Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Proper Technique; According To Rdc 185/2001; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Product Identification And Characteristics Information, Such As: Manufacturers Name, Product Validity Date, Name Of The Technical Responsible, Anvisa/Ms Registration; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Guarantee I, 07/23/2025