Compress, Operating Field, 100% Unleashed, Non-Sterile, Unique Use, Exempt From Impurities, Absent From Starch And Dextrin, Must Have A Device For Attachment In The Form Of Reach United To Your Body, Arranged In 04 Fixed Layers, Packed Edges, In The 23Cm X 25Cm Dimensions Without Pre-Enclosure. Follow Nbr 14767.Embalation: Package With 50 Units. Primary Packaged Individually In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfers With Techniqueseptic, Sterile And Apirogenic; The Primary Packaging Must Contain Product Identification And Characteristics Information, Such As: Name Of Manufacturer, Lot And Product Manufacturing Date, Sterilization Method, Sterilization Validity; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey Any Legislation That Sej, Dressing, Calcium Alginct, Carboxycholmethylcellulose And Silver Ions, Composed, At Least, By Guluronic Acid Or Other Seaweed Acids. Suitable For Highly Exudative Injuries And Light Bleeding Control. It Is Optional To The Presence Of Sodio. It Should Be Presented In Individual And Sterile Packaging, Size 10 X 10 (Variation Of + Or 1 Cm). Individual, Primary And Secondary Inbound Labeled According To Rdc 185/01 Anvisa. The Product Must Obey Any Current Legislation Regarding The., Crepom, Type I, Made With Cotton Wires And Mixed Fibers, 10Cm Wide Dimensions X 1, 80M Long, With 21, 8 Grams, With Twisted Or Simple Wire, With Elastic Properties In The Longitudinal, Jammed, Appearance, Appearance No Tears, Impurities, Lint, No Amendments, No Stains And Any Other Type Of Defect. Packed Individually, It Must Contain In A Legibly Fixed In Your Body Name And Product Brand, Composition, Manufacturer Identification, Shelf Life, Lot Number. Primary And Secondary Packaging Packed According To Current Standards. Present Anvisa., System, Closed Tracheal Aspiration System, For Use In Endotracheal Tube 08 Fr, Sterile, Apirogenic, Consisting Of Anti -Reflux Valve Irrigation, Attraumatic And Graduated Tube Probe, Covered By Siliconized Sheath Or Thin And Sturdy Protective Glove, Valve Of Safety Lock. Primary Packaging Packed According To Packaging Standards, Which Ensures The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Adequate Technique; The Label Label And/Or The Product Itself Must Contain Product Identification And Characteristic Information, Such As: Manufacturer Name, Lot, Manufacturing Date, Product Validity, Sterilization Validity; Name Of Technical Responsible, Anvisa/Ms Registration; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey, Tray, For Anesthesia, Containing: G 17 X 3 ¹/², Tuohy Bevel, Cm Scale, Luer Lock Translucido, Integrated Internal Mandrel; 1 Plastic Syringe With Loss Of Resistance, Luer Slip, 5Ml; 1 Circular Field Field With Paddress 10 Cm Standao And Adhesive Tape For Skin Fixation; 1 Paper Towel; 1 Syringe D
