Bids Are Invited For Acquisition Of Medical-Hospital Consumables And Radiodiagnostic Imaging Supplies (Drags, Hydrofibers, Thread, For Sutures, Njetor, Sclerosis Etc), To Form The Price Registration System.

Dressing, Made Of Hydrofibers, Grouped With 100% Sodium Carboxymethyl Cellulose And Ionic Silver, Dimensions 15 From The Product To The Time Of Use, Allow Openness And Transparency With Aseptic Technique, Externally Displaying Product Identification Data, Batch Number, Sterilization Validity Time Of At Least Two Years From The Date Of Sterilization, Manufacturer Identification Data, Registration Number With The Ministry Of Health. Upon Delivery, The Product Must Have An Expiration Date Of At Least 12 Months. The Secondary Packaging Must Be In Accordance With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use., Syringe, 03 Ml, With Needle 25 1 In 0.1 Mm., Numbered From 0.5 In 0.5 Ml, Plunger With Lubricated Piston And Adjusted To The Cylinder, Siliconized Needle, Atraumatic, Cylindrical, Straight, Hollow, With Trifaceted Bevel, Rigid And Centralized Without Burrs And Edges, With Needle Protector, Color Coded According To Nbr/ Isso10555-5. Polypropylene Cannon Allows For A Perfect Fit, Polypropylene Protector, Without Cracks And Well Attached To The Cannon. 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 Product Characteristics, Such As: Manufacturers Name, Batch And Date Of, Thread, For Suture, Chrome Catgut N. 2-0, Thread 70 Cm Long, (May Vary By + Or - 5Cm), Needle Of 4.0 Cm And 1/2 Circle, Cylindrical, (May Vary In + Or - 2Mm) Primary Packaging Individually Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Sterile And Pyrogenic. The Primary Packaging Must Contain Identification Information And Characteristics Of The Product, Batch, Manufacturing Date And Expiration Date. 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., Injector, Sclerosis, In Teflon, Sterile, With Or Without Side Washing, Dimensions 2.0 To 2.3 Mm(Diameter) 0.7 Mm In Diameter And 5 Mm To 8 Mm In Length And In The Other Two Or One Injector(S) For Cleaning And Injecting Medicines. Individual Packaging, Opening That Allows Opening With Aseptic Technique, With Identification Data Origin Date Of Manufacture Expiry Date And Registration With The Ministry Of Health.