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Dressing, Non-Adherent, Sterile, Composed Of A Woven Or Mesh Screen, Impregnated With Petrollatum Emulsion, Water-Soluble, In Roll Format, For Primary Coverage Of Open Wounds, Dimensions 07 Cm (Which Can Vary By Up To + 3 Cm) X 150 Cm (Which Can Vary By Up To + 50 Cm). Thermoplastic And Petala Opening. The Packaging Must Contain: Name And/Or Brand Of The Product, Batch And Date Of Manufacture, Expiration Date, Method Of Use, Restrictions On Use (When Necessary), Toxicological Information (When Necessary), Quantitative Indication, Manufacturer, Origin, Distributor And/Or Importer, Composition, Product Category, Type Of Sterilization (When Necessary), Technical Responsible, Registered With The Ministry Of Health., Of Collagen (90%), With Calcium And/Or Sodium Alginate (10%), Disposable, Single-Use, Absorbable, Flexible, Intended For Wounds With Moderate Exudation, Dimensions 10 Cm X 10 Cm And May Vary By Up To 2 Cm. 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 Comply With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use., Needle, For Spinal Anesthesia, Caliber 25 G Luer Lok, With Translucent And Entirely Conical Display That Guarantees Secure Connection. Individual Packaging, In Surgical Grade Paper And Thermoplastic Film And/Or Rigid Blister, Petala Opening. The Packaging Must Contain: Name And/Or Brand Of The Product, Type Of Sterilization, Registration With The Ministry Of Health, Hypodermic, Consisting Of A Stainless Steel Cannula, Size 1.2 Luer-Lock, Needle Protector Well Attached To The Barrel And Without Cracks, Sterile And Pyrogenic. Packaging That Allows Opening And Transferring With Appropriate Technique; Primary Packaging Must Contain: Manufacturers Name, Batch, Manufacturing Date, Product Expiration Date, Sterilization Method, Sterilization Validity, Name Of The Technical Person Responsible, Registration With Anvisa/Ms. Primary And Secondary Packaging Packaged And Labeled In Accordance With Current Legislation In Anvisa/Ms., Device, Connector, For Closed System, For Prolonged Use Of At Least 96 Hours, Which Does Not Allow The Use Of Needles, With Neutral Pressure System Preventing Blood Backflow, For Central, Peripheral And Arterial Lines, Compatible With Lipids, Blood And Cytostatics, Free Of Latex, Pvc, Dehp And Metal Parts, Which Allows At Least 200 Actuations, Access To All Types Of Catheters, Syringes And Equipment, With End Luer Lok Or Luer Slip, Non-Toxic, Disposable For Single Use. Packaging In Accordance With Standards That Guarantee The Integrity Of The Product Until The Moment Of Use. Present Registration Anvisa/Ms., 10/28/2025 - 18:30:56
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