Catheter, Umbilical, Neonatal, For Use In Neonatal Artery And Vein, Disposable, Radiopacus, Marking In A Cm Of Unique Lumen, Polyurethane, 2, 5 Fring Of 30 To 35 Cm. Thermoplastic, Opening In Petala. The Packaging Should Be Printed Identification Data, Procedure, Manufacturing Date, Type Of Sterilization, Expiration Date And Registration In The Ministry Of Health, Lamina, Scalpel Number 20, Sterile, In Stainless Stem, Without Burrs, With Sharp Cut And That Adapt To The Scalpel Cables Standard. 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 Technique; According To Rdc 185/2001; The Labeling Of The Primary Packaging And/Or The Product Itself Must Contain Product Identification And Characteristics, Such As: Manufacturer Name, Lot, Product Validity, Sterilization Method, Sterilization Validity; Name Of Technical Responsible, Anvisa/Ms Registration; 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. Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa., Connection, For Infusion, Simultaneous Of Solutions, In Non -Toxic, With Two Ways, Which Dispenses The Use Of Needles And Lids, Free Of Latex And Metal, Endowed With Closed System Filling Device. Primary Packaging Packaged Individually According To Packaging Standards, Which Ensures The Integrity Of The Product Until The Moment Of Its Use, Allowed Opening And Transfer With Proper Technique. Primarial Packaging Must Contain Identification And Characteristics Of The Product, Batch And Date Of Product Manufacturing, 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; Labeled According To Current Legislation. Following Security Standards According To Nr 32 (Annex I, Items 32.2, 32.3, 32.5)., Blood, Venous Line, For Hemodialysis, Adult, Unique Use, Pvc Flexible Tube, Jammed, With Catabolha, Filter Hydrophobic With Microbial Barrier (With Closed Lid), Clamp, Flow Cut, Threaded Connector, Autocycle Side Injector, Blue-Colored Connector, Semi-Rigid Connector Lid, Rigid Plastic; Luer Lok Connector With Rigid Plastic Lid; With Recirculator And Recirculation Lid, With Saline Entry Line. Packaged In Surgical Degree. Packaging That Ensures The Integrity Of The Product Until The Time Of Its Use Allowing The Opening And Transfer With Proper Technique. The Primary Packaging Label Must Contain: Manufacturer Name, Sterilization Validity, Name Of The Technicians Responsibility, Record At Anvisa/Ms. Pressed And Secondary Packaging Packages And Labeled According To Legislation In Force In Anvisa/Ms.
