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Dressing, Composed Of Fabric Impregnated With Activated Carbon And Silver, Wrapped By A Layer Of Non-Woven Fabric, Based On Low-Adhesion Nylon And Sealed Throughout Its Entire Length, Dimensions 20 Cm X 12 Cm And Can Vary By +/- 3 Cm. The Packaging Must Contain The Name And/Or Brand Of The Product, Batch And Date Of Manufacture, Expiration Date, Method Of Use, Restrictions On Use (When Necessary), Toxicological Information (When Necessary), Quantitative Indication, Manufacturer, Origin, Distributor And/Or Importer, Composition, Product Category, Type Of Sterilization (When Necessary), Responsible Technician, Registration With The Ministry Of Health, Barrier Cream, Skin Protector Against Effluents And Exudates, Moisturizer, Presented In Milliliters, With At Least 28 Ml. The Primary And Secondary Packaging As Per The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Time Of Use. The Product Must Comply With Any Legislation That Is Inherent To It, Inform Date Of Manufacture, Expiration Date, Anvisa Registration Number And Brand., Kit, Infusion, Central Venous, 2 Ways, Pediatric 3 Fr X (8 A10) Cm, Containing A Radiopaque Polyurethane Catheter, 0.18 Guide Wire, Syringe, Puncture Needle, Dilators And Secondary Fixation, Sterilized With Ethylene Oxide, Without Latex. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Opening In Petala. The Packaging Must Be Printed With Identification Data, Origin, Date Of Manufacture, Type Of Sterilization, Expiration Date And Registration With The Ministry Of Health, Tube, For Blood Collection, Vacuum, In Plastic, Transparent, Colorless, Sterile, With Separating Gel For Serum And Clot Activator, Aspiration Volume Of 5.0 Ml, Rubber Stopper Siliconized With Protective Plastic Cap In Red And/Or Yellow, Dimensions 13 X 100Mm. Labeled Tubes, Containing: Batch Number, Suction Volume And Manufacturers Brand, With Product Identification Data In Portuguese. Must Present Anvisa Registration
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