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Dressing Based On Essential Fatty Acids, Rich In Linoleic And Oleic Acids, Also Containing Capric, Caprylic, Lauric, Palmitic, Myristic, Stearic Acid, Retinol Palmitate (Vitamin A), Tocopherol Acetate (Vitamin E) And Soy Lecithin. Self-Drilling. Registration With Anvisa As A Risk Class Iii Correlate, With Indication For The Prevention And Treatment Of Wounds. The Packaging Must Contain The 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), Responsible Technician, Registration With The Ministry Of Health., Dressing, Made Of Hydrocellular Foam, Dimensions 09 Cm Vertical Absorption And The Third Layer Allows Gas Exchange, Impermeable To Water And Bacteria, Prevents The Return And Extravasation Of Absorbed Secretion, Avoiding Irritation Of The Skin Peri Cannula, With Fenestra And Orifice To Fit The Cannula Or Drain, Suitable For Protection Of Tracheostomies And Drains, Dressing Can Remain Without Handling Up To Seven Days. 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 A, Thread, For Suturing, For Single Use, In Blue Polypropylene, No. 2-0, 70 Cm Long (Can Vary By + Or - 5 Cm), Embedded With 01 Tapered Needle, Cylindrical Body, 1/2 Circle, 3.5 Cm Long (Can Vary By + Or - 2 Mm), For General Closure. Packaging: Primary Packaging Individually Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Up To The Moment Of Its Use, Allowing Opening And Transfer Using Aseptic, Sterile And Non-Pyrogenic Techniques; The Primary Packaging Must Contain Identification Information And Product Characteristics, Such As: Manufacturers Name, Batch, Manufacturing Date, Product Expiration Date, 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 It. Label, Device, Urinary, One Piece, In Natural Latex, Single Use, For Male Urinary Incontinence, Waterproof, Hypoallergenic, With Bulb-Shaped Lower End, Medium Size.Primary Packaging Individually Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use; The Printed Label Must Be Applied Directly To The Primary Packaging, And Must Contain The Following Information, Written In Portuguese: Manufacturers Name, Name And Brand Of The Product, Batch Code (Preceded By The Word Batch), Instructions For Use, Warnings Or Precautions For Use, Name Of Responsor
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