Bids Are Invited For Acquisition Of Medical-Hospital Consumables And Radiodiagnostic Imaging Supplies (Cathe ... in Brazil

Work Detail

Kit, Catheter, Central, Peripherally Inserted, 2.0 Fr Blood After Puncture With Safety System According To No. 3201 Measuring Tape01 Insertion Tweezers01 Anatomical Silicone Tourniquet01 Pvc Extender With Clamp Tweezers01 Luer Lock Connector With Lidprimary Packaging Individually Packed In Compliance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Use Allowing Opening And Transfer With Sterile And Non-Pyrogenic Aseptic Technology, The Packaging Must Contain Identification Information And Characteristics Of The Product, Such As The Name Of The Manufacturer, Batch, Date Of Manufacture, Validity Of The Product, Sterilization Method, Validity Of The Sterilization, The Secondary Packaging Must Comply With The Practice Of The Catheter For Hemodialysis, Long-Term, Straight, Single-Use, Disposable, Containing: 01 Catheter With Straight Extensions 15.5Fr 01 Introducer Needle 18G X 7 Cm; 01 Nitinol Metal Guide Wire 0.035 X 70 Cm In Jota; 01 Vein Dilator 12 Fr X 150 Mm; 02 Injection Caps; 01 Tunneling Trocar; 01 16Fr Valved Introducer. Individual Packaging In Surgical Grade Paper And Thermoplastic Film, Containing Identification Data, Origin, Type Of Sterilization, Date Of Manufacture, Expiration Date And Registration With The Ministry Of Health. You Must Present Anvisa Registration. The Product Must Comply With Any Current Legislation That Is Inherent To It., For Hemodialysis, Double Lumen, Sterile, Containing At Minimum: 01 Polyurethane Catheter With Straight Extensions 11 Fr Vein 12Fr Individual Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa. The Product Must Comply With Any Current Legislation That Is Inherent To It., 1.0 Fr Blood Reflux After Puncture; 01 Measuring Tape, Luer Lock Connector With Lid Primary Packaging Packed Individually In Compliance With Packaging Standards That Guarantee The Integrity Of The Product Up To The Moment Of Its Use, Allowing Opening And Transfer With Sterile And Pyrogenic Aseptic Tenon The Packaging Must Contain Identification Information And Characteristics Of The Product Such As Manufacturers Name Batch Date Of Manufacturing Product Validity Sterilization Method Sterilization Validity The Secondary Packaging Must Comply With The Manufacturers Practice In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use.

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