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Compress, Made Of 100% Cotton Gauze, Non-Sterile, For Single Use, Disposable, Hydrophilic, Free From Optical Bleaches And Starch, Must Have 05 Folds And 08 Layers Folded Inward, Dimensions Closed 7.5 Per Cm2. Follow Nbr13843.Packaging: Packages With 500 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 Inherent To It. Primari Packaging, Dressing, Non-Adherent, Sterile, Disposable, Single-Use, Composed Of A Woven Or Mesh Screen, Impregnated With Petrolatum Emulsion, Water Soluble, Intended For Primary Coverage Of Open Wounds, Dimensions 10 Cm X 20 Cm And May Vary In +/- 3Cm. Packaging Individually Packaged In Accordance With Rdc185/Anvisa On Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Use, Allowing Opening And Transparency With Aseptic Technique, Externally Showing Product Identification Data Batch Number Sterilization Validity Period Of At Least Two Years From The Date Of Sterilization Manufacturer Identification, 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., Crepe Bandage, Type Ii, Made With Cotton Threads And Mixed Fibers, Dimensions Of 15Cm Wide X 1.80M Long At Rest, Weighing 45.0 Grams, Coiled On Itself, With Twisted Or Single Thread, With Elastic Properties In The Longitudinal Direction, Non-Toxic, Uniform Appearance, Without Tears, Impurities, Lint, Without Seams, Without Stains And Any Other Type Of Defect. Individually Packaged, Must Contain The Name And Brand Of The Product, Composition, Manufacturer Identification, Expiration Date, Batch Number, Legibly Fixed On The Body. Present Certificate Of Registration With Anvisa. Individual Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa. The Product Must Comply With Current Legislation., Syringe, 60 Ml, Without Needle, Catheter Type Nozzle, Made Of Polypropylene, Transparent, Non-Pyrogenic, Straight Siliconized Cylinder, Uniform Wall, With Graduation Scale In Ml, Legible Numbers And Lines, With Retaining Ring That Prevents The Detachment Of The Plunger From The Cylinder, Nozzle Without Thread That Guarantees Safe Connections, Flange With Appropriate Shape, Piston With Lubricated Piston And Adjusted To The Cylinder. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Petala Opening. The Packaging Must Be Printed: Product Identification Data, Origin, Batch And Date Of Manufacture, Type Of Sterilization And Registration With The Ministry Of Health., Glove, Surgical, Number 8, 0, In Natural Latex, Uniform Texture, Anatomical Shape, Resistant To Traction, Cuff With Sheath, Minimum Length Of
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