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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 30.0Cm, Density Of 13 Threads 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 Techniques; 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 M, Crepe Bandage, Type Ii, Made With Cotton Threads And Mixed Fibers, Dimensions Of 25Cm Wide X 1.80M Long At Rest, With 75.0 Grams, Coiled On Itself, With Twisted Or Single Thread, With Elastic Properties In The Longitudinal Direction, Non-Sterile, Non-Toxic, Uniform Appearance, Without Tears, Impurities, Lint, Without Seams, Without Stains And Any Other Type Of Defect. Individually Packaged, Must Contain, Legibly Fixed On The Body, The Name And Brand Of The Product, Number Of Threads Per Cm, Composition, Manufacturer Identification, Expiration Date, Batch Number, Name Of The Responsible Technician And Registration Number, Registration Number From The Record Of The Ministry Of Health, According To Resolution Rdc No. 185 Of Anvisa, Resolution No. 02 Of 12/31/2001 Of Conmetro, Ordinance No. 157 From Inmetro And Nbr 14056., Bandage, Made Of Hydrofibers, Dimensions 15 Packaging Individually Packaged In Accordance With Rdc185/ Anvisa On Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transparency With Aseptic Technique, Externally Showing Product Identification Data Batch Number Validity Time Of Sterilization Of At Least Two Years From The Date Of Sterilization Manufacturers 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 Comply With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use., Thread, For Suture, In Polyglactin Or Polyglycolic Acid, Violet, Absorbable, Locked, N. 3- 0, 70 Cm Long Thread (Variation Of + Or - 5 Cm), Needle 3.0 Cm (Variation Of + Or 3 Mm), 1/2 Cylindrical, Gastrointestinal. 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., Syringe, 3Ml, With Safety Device, Coupled With Needle Dimensions Of 25 Retention That Prevents Detachment Of The Cylinder Piston, Flange With Appropriate Shape, Piston With Lubricated Piston And Adjusted To The Cylinder. You Must Present Anvisa Registration.
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