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Visco/Polyester Non-Woven Dressing, Impregnated With 20% Sodium Chloride For Use On Non-Infected Wounds, Moderate To High Exudate Level, Cuttable. Dimensions 10X10 Cm. Presentation Containing Identification Information, Product Characteristics, Brand And Anvisa Registration. Primary And Secondary Packaging Labeled In Accordance With Current Legislation., Bottle, For Chest Drainage, Sterile, Disposable, Consisting Of A Reservoir Bottle With A Capacity Of 1000 Ml, Graduated Every 50 Ml, 20 Cm Mariot Tube, Screw-Sealing Lid, Fixing System To The Bed Using A Plastic Tube And Positioning Support Vertical.Individual Packaging, In Surgical Grade Paper And Thermoplastic Film, Opening In Petala. The Packaging Must Be Printed With Identification Data, Type Of Sterilization, Origin, Date Of Manufacture, Expiration Date And Registration With The Ministry Of Health., Syringe, Hypodermic, Single Use, For Manual Use, 1.0 Ml, With Needle Of Minimum Dimensions Of 10 Needle Protector, Made Of Polypropylene, Transparent, Siliconized, Non-Toxic, Non-Pyrogenic, Uniform Wall, Straight Cylinder, Retaining Ring That Prevents Plunger Detachment, Threadless Nozzle That Guarantees Secure Connections, Flange In Appropriate Shape, Piston With Lubricated Piston And Adjusted To The Cylinder, With Millimeter Graduation Scale, Legible Numbers And Dashes. Individual Primary Packaging, Opening In Petals, Which Guarantees The Integrity Of The Syringe, Especially Regarding The Maintenance Of The Sterility Of The Contents In Accordance With Rdc/03/2011/Anvisa; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Such As: Name Of The Manufacturer, Batch, Sterilization Expiration Date, Name Of The Person Responsible For Technology, Cannula, Wired Endotracheal, No. 8, 5, In Transparent Pvc, With Opaque Cuff, High Volume And Low Pressure Balloon, Semi-Assembled Connector, Retracted Atraumatic Tip, Continuous Radiopaque Line, Graduated Marks Indicating Depth Through The Cannula Body And Caliber Marked In A Single Location, Non-Toxic. Packaging That Allows Opening And Transferring With Appropriate Technique; The Primary Packaging Label Must Contain: Manufacturers Name, Manufacturing Date, Product Expiry 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 At Anvisa/Ms., Probe, Urethral, N. 12, Malleable, Pvc, Atraumatic, Silicone, With Universal Connector With Lid. 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., 11/26/2025 - 18:30:57, Thread, For Suture, In Polydioxanone, N 5-0, With 70 Cm Long (Variation Of + Or - 5 Cm), 17Mm Needle (Variation Of + Or - 02 Mm) And ½ Cylindrical Circle. Individual Packaging Must Be Printed With Identification Data, Date Of Manufacture, Expiration Date And Registration With The Ministry Of Health. Must Comply With Current Legislation/Technical Standards., Nasal Cpap, Childrens, Number 0, Composed Of: 01 Nasal Prong In 100% Silicone, With Anatomical Fit And Two Side Openings; Corrugated Trachea 40 Cm Long With Connection; Two Flexible And Transparent Corrugated Tracheas With At Least 120 Cm Long, With Connections; Line
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