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Needle, Hypodermic, 40 Individual, On Surgical Grade Paper And/Or Thermoplastic Film, Petala Opening. The Packaging Must Be Printed With Identification Data, Origin, Date Of Manufacture, Type Of Sterilization, Expiration Date And Registration With The Ministry Of Health, Thread, For Suture, In Linen No. 2-0, Thread 15 X 45 Cm Long, Without Needle. Packaging: Individual Envelope, In Aluminum Foil Or Surgical Grade Paper And/Or Film Thermoplastic, Expiry Date And Registration With The Ministry Of Health., Intravascular Catheter For Peripheral Puncture No. 16G, Outside The Needle Type, Single Use, Non-Toxic, Non-Pyrogenic, Radiopaque, Medium-Permanence Consisting Of Stainless Steel Needle, Siliconized Atraumatic With Short Biangulated And Trifaceted Bevel, Precisely Sharpened, Without Burrs And Edges, Catheter In Flexible Polyurethane Biomaterial, Transparent (Radiopaque) Needle Protector, Luer Lok Connector Catheter, Translucent, Color Coded According To Nbr 10555-5, With Slots For Fixation, Transparent Plastic Reflux Chamber, Allowing Rapid Visualization Of Blood Reflux And Cover, Filter Hydrophobic, Safety Device In Accordance With No. 32. Individually Packed Using A Sterilization Method That Allows Opening And Aseptic Transfer, Maintaining The Integrity Of The Product And Its Sterilization Until The Time Of Use. Must Contain Externally On The Packaging The Batch No., Sterilization Method Compatible With, Device, Urinary, For Urinary Incontinence, Male, In Special Medical Plastic (Not Latex), Sheath Type, 1 Piece System (Self-Adhesive), 35 Mm With A Margin Of 1 Mm More Or Less. Supply Unit: Unit. Packaging With Product Identification Data, Manufacturers Brand And Registration With The Ministry Of Health., Scalpel Blade, Number 22, In Stainless Steel, Without Burrs, With A Sharp Cut And That Adapts To Standard Scalpel Handles. Primary Packaging Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Use, Allowing Opening And Transfer With Aseptic Technique; According To Current Legislation; 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, Anvisa/Ms Registration; 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 Any Legislation That Is Inherent To It. Primary And Secondary Packaging Labeled According To Current Legislation., 02/04/2026 - 18:30:48
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