Bids Are Invited For Acquisition Of Medical And Hospital Consumer Materials, With Aim To Meet The Needs Of Inácia Pinto Dos Santos Hospital.

Compress, Sterile Operating Drape 25 Cm It Must Have A Device For Fixing It In The Form Of A Strap Attached To Your Body, With A Radiopaque Element Fixed To Your Body. It Must Be Arranged In 04 Layers Fixed To Each Other, Edges Sheathed, In Dimensions 25 Cm X 28 Cm With Pre-Shrinkage. The Requirements And Guidelines Of The Abnt Nbr 14767:2009 Standard Must Be Complied With. Presentation: Sterile Primary Packaging In The Form Of A Package With 05 Units Inside Each. Each Primary Packaging Must Contain The Product In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use. The Primary Packaging Must Allow Opening And Transfer Using Aseptic, Sterile And Non-Pyrogenic Techniques. 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, Product Expiration Date, And Anvisa Registration. The Secondary Packaging Must Have A Security Seal To Protect And Guarantee The Integrity Of The Product During Transport, Storage And Until The Moment Of Use. The Product Must Comply With Any Legislation Inherent To It. The Primary And Secondary Packaging Must Be Labeled According To Rdc Anvisa No. 751/2022., Gauze Compress 7.5 Cm Optics, Starch And Impurities In General. It Must Have 05 Folds, 08 Layers Folded Inwards, With Dimensions When Closed Of 7.5 Cm, With Dimensions When Opened Of 15 Cm X 30 Cm And With A Density Of 13 Threads Per Cm2. The Requirements And Guidelines Of Abnt Nbr 13843:2009 And Abnt Nbr 13841:2016 Must Be Complied With. Presentation: Primary Packaging In The Form Of A Package With 10 Units Of The Product. Each Primary Packaging Must Contain The Product In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use. The Primary Packaging Must Allow Opening And Transferring With Aseptic Technique, Such As: Product Description, Manufacturers Name, Expiry Date, Anvisa Registration. The Secondary Packaging Must Have A Safety Seal For Protection And To Guarantee The Integrity Of The Product During Transportation, Macrodrops Equipment (Sterile For Intravenous Solution With Gravity Infusion And Apyrogenic, With Protective Cap At The Entrance And Exit, Tri-Faceted Piercing Tip, Adaptable To Any Type Of Parenteral Solution Bottle, Air Inlet With Hydrophobic And Bactericidal Membrane, Drip Chamber Transparent, Flexible And With Polymeric Filters, Non-Toxic Pvc Extension Tube With 1.50Cm And Roller Clamp With Flow And Rest Chart, With Good Glide And Allowing Precise Control Of The Infusion Flow, Side Injector With Finger Protector And Self-Healing Infusion Points, Even After Being Pierced Several Times With A 40Mmx 1 Gauge Needle, 2Mm, Non-Leaking, Luer Lock Intermediate Connector, Reversible And Adaptable To Any Type Polymer, Individually Packed In Surgical Grade Paper And Thermoplastic Film With Opening In Petals And Identification Data, Type Of Sterilization, Origin, Date Of Manufacture, Batch Number And Manufacturer Registration With The Ministry Of Health, In Compliance With Rdc Resolution No.