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Dressing, Fixator For Peripheral Catheter, Composed Of Semipermeable Polyurethane Film, Transparent, Fenestrated, Sterile, Flexible, Adherent, With Permeability To Oxygen And Water Vapors, Dimensions 7 Cm X 9 Cm, Which Can Vary By +/- 1 Cm, With Extra Strips To Stabilize The Catheter. Packaging: Primary Packaging Individually Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Aseptic, Sterile And Pyrogenic Technique; The Printed Label Must Be Applied Directly To The Primary Packaging, And Must Contain The Following Information, Written In Portuguese: Manufacturers Name And Product Brand, Batch Code, Date Of Manufacture, Expiry Date, Anvisa/Ms Registration, Name Of The Technical Person Responsible. Secondary Packaging Must Be In Accordance With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Time Of Use., Macrodrops Equipment For Enteral Feeding, With Protective Cap At The Entry And Exit, Three-Faceted, Perforating Lancet, Adaptable To Diet Bottles, Air Inlet With Hydrophobic And Bactericidal Membrane, Flexible And Transparent Drip Chamber, Pvc Extension Tube And With A Caliber Suitable For Craft Diet, Nontoxic, With Roller Gripper And Adaptable To Any Type Of Probe. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Opening In Petala. Identification Data, Type Of Sterilization, Origin, Date Of Manufacture, Expiration Date And Registration With The Ministry Of Health Must Be Printed On The Packaging. Irrigation System With Anti-Reflow Valve, Atraumatic And Graduated Tip Probe, Covered By Siliconized Sheath Or Thin And Resistant Protective Glove, Suction Valve With Safety Lock. Primary Packaging Packed In Accordance With Packaging Standards, Which Guarantees The Integrity Of The Product Until The Moment Of Use, Allowing Opening And Transfer With Appropriate Technique; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Such As: Manufacturers Name, Batch, Product Expiration Date, Sterilization Method, Sterilization Validity; Name Of The Technical Person Responsible, Registration With Anvisa/Ms; Secondary Packaging Must Comply With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use; The Product Must Comply With The System For Use In A 12 Fr Endotracheal Tube, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use;, For Use In A 16 Fr Endotracheal Tube, In Order To Guarantee The Integrity Of The Product During Storage Until Use; The Product Must Comply, 12/11/2024 - 18:30:37
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