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Colorless Gel, Moisturizer Composed Of Carboxymethylcellulose, Calcium And Sodium Alginate, Propylene Glycol, Carbomer 940, Triethanolamine, Boric Acid, Hydantoin And Potassium Sorbate, Amorphous, Minimum 85 Grams. Presentation Containing Identification Information, Product Characteristics, Brand And Anvisa Registration. Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa. The Product Must Comply With Current Legislation. Ref. Saeb 65.10.19.00125939-3, Scalpel Blade Number 15, Disposable, Sterile, Stainless Steel, Burr-Free, With Sharp Cutting And Adapting To Standard Scalpel Handles. Primary Packaging Packed In Accordance With Packaging Standards That Guarantees The Integrity Of The Product Until The Moment Of Its 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 Method, 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 According To Rdc 185/01/Anvisaref. Saeb 65, Cannula, For Pvc Tracheostomy, Non-Toxic, Number 7.0, With High Volume And Low Pressure Cuff, Balloon With Connector For Leur And Leur-Lock Syringes, Continuous Radiopaque Line, Obturator Cap, Atraumatic Tip And Cannula Fixation Tape . 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. The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Anvisa/Ms Registration. 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. The Product Must Comply With Any Legislation That Is Inherent To It. Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa., Device, Urinary, For Urinary Incontinence, Male, In Special Medicinal Plastic (Non-Latex), Sheath Type, 1 Piece System (Self-Adhesive), 40 Mm With Margin 1 Mm More Or Less. Supply Unit: Unit. Packaging With Product Identification Data, Manufacturers Brand And Registration With The Ministry Of Health. Ref. Saeb 65.15.19.00113587-2, Anvisa Brand And Registration. Primary And Secondary Packaging Labeled According To Rdc 185/01/Anvisa. The Product Must Comply With Current Legislation.Ref. Saeb 65.10.19.00125939-3 Rc, 16/01/2025, Manufacturers Mark And Registration With The Ministry Of Health.Ref. Saeb 65.15.19.00113587-2 Rc
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