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10Ml Syringe Without Needle, Disposable, Sterile, Polypropylene, Transparent, Non-Toxic, Non-Pyrogenic, Straight Cylinder, Siliconized, Uniform Wall, Retaining Ring That Prevents Detachment Of The Cylinder Plunger, Threadless Nozzle That Guarantees Secure Connections, Flange That Supports The Fingers, Plunger With Lubricated Piston And Adjusted To The Cylinder, With Graduations In Ml, Numbers And Legible Lines. Individual Packaging, In Surgical Grade Paper And/Or Thermoplastic Film, With Petal Opening, With Identification Data, Origin, Date, Type Of Sterilization, Expiration Date And Registration With The Ministry Of Health., Connection, Neonatal, For Simultaneous Infusion Of Solutions, With Two Ways, Identified By Colors, With Adaptation According To Nbr - That 594 - 1 E 2, Which Eliminates The Use Of Needles And Caps, Free Of Metal And Equipped With A Device For Filling A Closed System, Free Of Pvc. Packaging: Individually Packaged In Accordance With Rdc 185/Anvisa On Packaging Standards, Which Guarantees The Integrity Of The Product Until The Moment Of Use, Allows Opening And Transfer With Aseptic Technique, Externally Containing Data From Product Identification, No. Batch, Sterilization Expiry Time Of At Least Two Years From The Sterilization Date, Manufacturer Identification Data, No. Ministry Of Health Registration. Follow Safety Standards In Accordance With Nr 32 (Annex I, Items 32.2, 32.3, 32.5). Upon Delivery, The Product Must Have An Expiration Date Of At Least 12 Months., Tracheal Aspiration Probe, No. 08, For Single Use, Malleable, In Pvc, Atraumatic, With 01 Distal Hole, 02 On The Sides And Universal Connector. Primary Packaging Individually Packaged In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Aseptic Technique; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Information, Written In Portuguese: Manufacturers Name, Product Name And Brand, Batch Code, Manufacturing Date, Expiry Date, Composition, Sterilization Method, Sterilization Validity, Registration Number With Anvisa/Ms, Name Of The Technical Responsible Person; 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. Primary And Secondary Packaging Must Be Labeled In Accordance With Current Anvisa Legislation. The Product Must Comply With Q, Needle, For Aspiration Of Solutions, Composed Of Stainless Steel Cannula, Lubricated, Dimension 1.2 Cracks, Sterile And Non-Pyrogenic. Packaging That Allows Opening And Transferring With Appropriate Technique; Primary Packaging Must Contain: Manufacturers Name, Batch, Product Expiry Date, Name Of Technical Responsible, Registration With Anvisa/Ms. Primary And Secondary Packaging Conditioned And Labeled According To Current Legislation At Anvisa/Ms., 03/12/2025 - 18:30:53
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