Bids Are Invited For Acquisition Of Hospital Medical Material (Closed Tracheal Aspiration System, Canula, For Pvc Tracheostomy, Etc), To Form The Price Registration System.

Closed Tracheal Suction System, For Use In A 14 Fr Endotracheal Tube, Consisting Of An Irrigation Line With Anti-Reflux Valve, Probe Covered By A Silicone Sheath, Suction Valve With Suction Lock. Individual Packaging. The Packaging Must Contain: Name And/Or Brand Of The Product, Expiration Date, Method Of Use, Use Restrictions (When Necessary), Toxicological Information (When Necessary), Quantitative Indication, Manufacturer, Origin, Distributor And/Or Importer, Composition, Product Category, Responsible Technician And Registration With The Ministry Of Health/Anvisa, Cannula, For Tracheostomy Made Of Pvc, Disposable, Sterile, Non-Toxic, Number 4.5, With High Volume And Low Pressure Cuff, Balloon With Connector For Leur And Leur-Lock Syringes, Continuous Radiopaque Line, Obturator Cap, Atraumatic Tip And Cannula Fixation Tape. 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. The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Such As: Name Of The Manufacturer, Batch, Date Of Manufacture, Expiration Date Of The Product, Anvisa/Ms Registration. 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. The Product Must Comply With Any Legislation That Is Inherent To It. Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa., Button, For Gastrostomy, Dimensions 20 Fr X 2.5 Cm, ​​In Silicone, With Kit For Sterile Implantation. Primary Packaging That Allows Opening And Transfer With Appropriate Aseptic Technique. You Must Present Anvisa Registration. Individual Primary Packaging And Secondary Packaging Labeled According To Rdc 185/01/Anvisa., Catheter, For Central Venous Access, Double Lumen, Caliber 5Fr Lumens, Not Generating Occlusion Due To Drug Incompatibility, High Flow, With Exits Located At Different Points Of The Catheter, Made Of Polyurethane, Totally Radiopaque, With Depth Graduation In Centimeters, Soft Tip With Cone-Shaped Design, Insertion Using Seldinger Technique, Guide Wire With Distal J Tip And Protective Cap, Introducer Needle, 5Cc Syringe, With Holding Handles And Clamps. Individual Primary Packaging And Secondary Packaging Labeled According To Current Legislation. Present Anvisa Registration Certificate. The Product Must Comply With Current Legislation, For Tracheostomy, Metalica, Nº 05. Must Present Anvisa Registration. Packaging Conditioned In Accordance With Current Regulations.