Bids Are Invited For Acquisition Of Medical-Hospital Consumables And Radiodiagnostic Imaging Supplies (Folley Probe, Suture Thread, Guedel Cannula, Etc), To Form The Price Registration System.

Probe, Folley, N. 10, 02 Ways, 5 Cc Balloon, Sterile, In Natural Rubber Of Appropriate Shape, Siliconized, With Anti-Fouling, Rounded Proximal Tip, With Large, Rounded And Smooth Holes. 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. Units. The Packaging Must Be Printed With Identification Data, Cannula, Guedel, No. 03, Disposable, Made Of Non-Toxic Material, Flexibility And Adequate Curvature, Central Hole That Guarantees Ventilation, With A Safety Edge, Resistant To Disinfection, With Numbers On The Edge To Identify The Size And Be Transparent White For Viewing. Secretion. 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 Rdc 185/2001; 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; The Secondary Packaging Must Be In Accordance With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Present, Of Tracheal Aspiration, N. 18, For Single Use, Non-Toxic, Malleable, In Pvc, Transparent, Atraumatic, With 01 Distal Hole, 02 On The Sides And Universal Connector. Primary Packaging Individually Packaged In Accordance With Packaging Standards That Guarantee Product Integrity Up To The Moment Of 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, Expiry Date, Composition, Sterilization Validity, Registration Number With Anvisa/Ms, Name Of The Technical Person Responsible; 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, Hypodermic, For Insulin Pen, Composed Of Stainless Steel Cannula, Dimension 0.25 Packaging That Allows Opening And Transferring With Appropriate Technique; Primary Packaging Must Contain: Manufacturers Name, Date Of Manufacture, Sterilization Method, Validity Of Sterilization, Name Of The Technical Person Responsible, Registration With Anvisa/Ms. Primary And Secondary Packaging Packaged And Labeled In Accordance With Current Legislation In Anvisa/Ms., System, Collector, Secretion, For Bronchoscopy And Endoscopy, Composed Of: Bottle, Made Of Non-Toxic Pvc, Rigid And Graduated In Millimeters; Lid With Full Thread, In Polypropylene, With 02 (Two) Ways And Non-Toxic Pvc Handle; Polypropylene Adapter Fixed To The Lid; Handle For Transport And Fixation; Label