Bids Are Invited For Acquisition Of Medical-Hospital Material, Through A Price Registration System To Meet The Needs Of Fesf-Sus.

Closed Tracheal Aspiration System, For Use In 08 Fr Endotracheal Tube, Consisting Of Irrigation Path With Anti-Reflow Valve, Probe Covered By Siliconized 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, For Use In 10 Fr Endotracheal Tube, For Use In 12 Fr Endotracheal Tube, Responsible Technician And Registration With The Ministry Of Health/Anvisa., For Use In 14 Endotracheal Tube Fr, Tracheal Aspiration Probe, N. 12, Disposable, Single Use, Sterile, Non-Toxic, Malleable, Pvc, Transparent, Atraumatic, With 01 Distal Hole, 02 On The Sides And Universal Connector. 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: Manufacturers Name, Batch, Manufacturing Date, Product Expiration Date, Sterilization Method, Sterilization Expiration Date; 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 Rdc 185/01/Anvisa., 09/06/2024, N. 14, In Transparent Pvc, With Holes And Universal Connector. Primary And Secondary Packaging In Accordance With Current Packaging Standards. Present Anvisa Registration, N. 16, Transparent White, Siliconized, 02 On The Sides And Universal Connector With Cover. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Opening In Petala. The Packaging Must Be Printed With Identification Data, Type Of Sterilization, Origin, Expiration Date And Registration With The Ministry Of Health., De Folley, N. 18, In Soft Latex, 02 Copies, 30 Ml Bottle. Primary And Secondary Packaging In Accordance With Current Packaging Standards. Present Anvisa Registration, N. 22, 30 Ml Pack, Steril. Individual Packaging, Urethral, ​​Silicone, With Universal Connector With Cap. You Must Present Anvisa Registration. Individual Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa. The Product Must Comply With Any Current Legislation That Is Inherent To It., N. 04, 02 On The Sides And Universal Connector. Primary Packaging Individually Packed 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, Sterilization Validity, Anvisa/Ms Registration Number, Name Of Person Responsible Technical; 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.