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Connection, For Simultaneous Infusion Of Solutions, With Two Routes, Which Eliminates The Use Of Needles And Caps, Free Of Metal And Equipped With A Device For Filling A Closed System. 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, Sterile And Non-Pyrogenic Technique; The Primary Packaging Must Contain Identification Information And Characteristics Of The Product, Such As: Name Of The Manufacturer, Batch And Date Of Manufacture Of The Product, Sterilization Method, Sterilization Validity; 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 Rdc 185/01/Anvisa., Tube, Endotracheal, With High Volume And Low Pressure Balloon, With Cuff No. 7, Disposable, Sterile, Pvc, Transparent, Non-Toxic, With Balloon With Conical Shape That Prevents Microaspiration, With Specific Lumen For Sub-Glottic Aspiration, Cuff Opaque, Retracted Atraumatic Tip With Murphys Eye, Thermosensitive, Continuous Radiopaque Line, Magill Curve, With Pilot Balloon And Valve, Graduated Marks Indicating Depth Through The Cannula Body And Gauge Marked In A Single Location On The Cannula. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Opening In Petala. Identification Data, Origin, Date Of Manufacture, Type Of Sterilization, Expiry Date And Registration With The Ministry Of Health Must Be Printed On The Packaging. Millimetrated And Numbered Graduation, Legible Numbers And Dashes, Luer Lock Nozzle, Uniform Wall, Retaining Ring That Prevents Detachment Of The Plunger, Compatible With All Brands Of Needles, Anatomically Shaped Flange, Must Comply With Rdc/03/2011/Anvisa, Primary Packaging Packed In Accordance With The Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Use, Allowing Opening And Transfer With Appropriate Technique; The Primary Packaging Label Must Contain Identification Information And Characteristics Of The Product, Batch, Product Expiration Date, Sterilization Expiration Date; Name Of The Technical Person Responsible, Anvisa/Ms Registration; Secondary Packaging Must Comply With Industry Practice
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