Bids Are Invited For Acquisition Of Hospital Medical Material (Dressing, Wire And Urinary Device), To Compose The Price Registration System.

Curative, In Antiseptic Gel For Wound Use, Composed Of Polyhexanide (Phmb) To 0, 1%, 0 0, Cellulose And/Or Cellulose Derivatives, With Humectant, Emollient, Debride And Anesthesic Properties. Hypoalogical, Bactericidal, Sports, Fungicidal And Viricidal Action, Including Staphylococcus, Pseudomonas And Salmonellas, Cutanea Compatibility Report. 100 G Tube Presentation. 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 Asptic And Apirogenic Technique; Primary Packaging Must Contain Information Identification And Characteristics Of The Product. Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey Any Legislation That Is Inherent In It. Labeling: Primary And Secondary Packaging Rotulated Legis, Wound Use Gel, Composed Of Carboxymethylcellulose, Alginate And Propylene Glycol, Tube With 85G. Packaging Individually Packed According To Rules In Force In Anvisa, Which Ensures The Integrity Of The Product Until The Moment Of Its Use, Allow Opening And Transfers With Asptic And Apirogenic Technique And Containing Product Identification And Characteristics Data, Batch Number, Manufacturer Identification Data And Registration Number In The Health Ministerium. Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure Product Integrity During Storage Until The Time Of Use. Supply Unit: 85G Tube, Suture, Sterile, Unique, Blue Polypropylene, 70 Cm Long (May Vary At + Or - 5 Cm), Cylinder -Ended, 1/2 Needle, 1/2 Needle Circle, With 3, 5 Cm Long (Can Vary At + Or - 2 Mm) For General Closure. Packaging: Primary Packaging Packaged Individually According To Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Asptic, Sterile And Apirogenic Technique; The Primary Packaging Must Contain Product Identification And Characteristics Information, Such As: Manufacturer Name, Lot, Manufacturing Date, Product Validity, Sterilization Method, Sterilization Validity; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey Any Legislation That Is Inherent In It. Rotula, Device, Urinary, For Urinary Incontinence, Masculine, Disposable, In Special Medicinal Plastic (Non -Latex), Sheath Type, System 1 Sin (Self -Adhesive), 35 Mm With 1 Mm Margin To Plus Or Less. Supply Unit: Unit. Packaging With Product Identification Data, Manufacturer Brand And Registration In The Health Ministry.