Bids Are Invited For Acquisition Of Materials And Equipment. For Hospital, Dental, Veterinary And Laboratory Use (Compress, Device, Equipment, Etc), To Compose The Price Registration System.

Compress, Made Of 100% Cotton Gauze, Sterile, For Single Use, Disposable, Hydrophilic, Free From Optical Bleaches And Starch, Must Have 05 Folds And 08 Layers Folded Inwards, Closed Dimensions Of 7.5 X 7.5 And Open Of 15. 0 X 30.0 Cm, Density Of 13 Strands Per Cm2. Follow Nbr 13843. Presentation: Packaging Packaging: Packs Of 10 Units, Primary Packed Individually According To 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 Characteristics Of The Product, Such As: Manufacturers Name, Batch And Date Of Manufacture Of The Product, Sterilization Method, Sterilization Validity; 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 The Device, Urinary, For Urinary Incontinence, Male, Disposable, In Special Medical Plastic (Non-Latex), Sheath Type, 1 Piece System (Self-Adhesive), 30 Mm. Packaging: Box With 30 Units, With Product Identification Data, Manufacturers Brand And Registration With The Ministry Of Health., Scalpel Blade Number 24, In Stainless Steel, Without Burrs, With A Sharp Cut And That Adapt To Scalpel Handles Standard. 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, Manufacturing Date, Product Expiration Date, 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 In Accordance With Rdc 185/01/Anvisa, Equipment, Macrodrops For Intravenous Solution For Infusion By Gravity, Non-Pyrogenic, Single Use, With Protective Cap At The Inlet And Outlet, Three-Faceted Piercing Tip, Adaptable To Any Type Of Parenteral Solution Bottle , Air Intake With Hydrophobic And Bactericidal Membrane, Chamber Transparent, Flexible Drip, With Particle Filter, Pvc Extension Tube With A Minimum Length Of 1.50 M, Roller Gripper With Good Glide And Allowing Precise Control Of The Infusion Flow, Self-Healing Side Injector Even After Being Pierced Several Times With A Needle 40 X 12 Gauge, Latex Free And Adaptable To Any Type Of Catheter. Packaging That Allows Opening And Transferring With Appropriate Technique; The Label Of The Primary Packaging And/Or The Product Itself Must Contain: Name Of The Manufacturer, Sterilization Validity Period, Name Of The Technical Person Responsible, Registration With Anvisa/Ms. Primary And Secondary Packaging Packaged And Labeled With, Electrode, Adult For Continuous Cardiac Monitoring And Electrocardiogram, Compatible With Any Monitor, Non-Sterile, Single-Use, Made Of Foam/Rubber. Adhesive, Hypoallergenic Bottom Side With Solid Conductive Gel. Stainless Steel Pin System, Counter-Pin Silver/Silver Chloride ( Ag/