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Dressing, Formed By A Self-Adhesive Silicone Layer For A Gentle Fit And Atraumatic Removal, Does Not Adhere To Damp Surfaces, Absorption Layer Formed By A Polyurethane Foam And Retention Layer Made Up Of Cellulose Particles That Transform The Absorbed Exudate Into Gel. External Film Impermeable To Water, Allowing Gas Exchange, Hypoallergenic, Flexible, Sterile, Single-Use, Disposable, Dimensions 15 X 15 Cm, With Regular Formats, Which Can Vary By + Or Minus 2 Cm. Identification Data, Origin, Date Of Manufacture, Type Of Sterilization, Expiry Date And Registration With The Ministry Of Health Must Be Printed On The Packaging., Catheter, Intravascular, For Peripheral Puncture, No. Stainless Steel Needle, Atraumatic, Siliconized With Biangulated And Trifaceted Bevel, Precisely Sharpened, Without Burrs And Edges, Catheter In Polyurethane Biomaterial, With Needle Protector, Luer Lock Connector, Translucent, Color Coded According To Nbr 10555-5, With Slots For Fixation, Transparent Reflux Chamber, Allowing Rapid Visualization Of Blood Reflux. Packaging: Individually Packaged In Accordance With Rdc 185/Anvisa On Packaging Standards, Which Guarantees The Integrity Of The Product Until The Moment Of Use, Allows Opening And Transfer With Aseptic Technique, Externally Containing Product Identification Data, No. Batch, Sterilization Expiry Time Of At Least Two Years From The Sterilization Date, Identification Data Of The Syringe, 01 Cc, Graduated From 0.01 Into 0.01 Ml, Numbered From 0.1 To 0.1 Ml, Attached With A 13 X 3. 8 Or 13 X 4 Needle, 5 Mm, In Polypropylene, Transparent, Non-Toxic, Non-Pyrogenic, Straight Cylinder, Siliconeized, Uniform Wall, With Retaining Ring That Prevents The Piston From Detaching From The Cylinder, Flange With A Suitable Shape, Piston With Lubricated Piston And Adjusted To The Cylinder. Packaging That Allows Opening And Transfer With Appropriate Technique; The Label Of The Primary Packaging And/Or The Product Itself Must Contain: Name Of The Manufacturer, Batch, Expiration Date Of The Product, Sterilization Method, Sterilization Expiration Date, 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. Supply Unit: Unit, Filter, Humidifier, For Adult Use, Respiratory, Heat And Humidity Exchanger, For Use With Pulmonary Ventilators, Hygroscopic Type Filter, Associated With A Viral And Hydrophobic Bacterial Filter, With Current Volume Of The Following Range: Lower Value Of The Range Of At Least Between 150 Ml, And Upper Value Of The Range Of No Maximum 1500 Ml, Non-Pyrogenic And Single Use. Must Have Internal Dead Space In Compliance With Regulatory Standards For This Product. Sterile Flexible Tube Must Accompany The Product. Primary And Secondary Packaging In Accordance With Current Packaging Standards. Present Anvisa Registration., Blood Collection Tube, Vacuum, With 3.2% Sodium Citrate Anticoagulant, Aspiration Volume Between 1.8 To 2.5Ml, Disposable And Sterile Transparent Plastic Material, With Double Wall That Prevents The Evaporation Of The Anticoagulant, And Protects The Vacuum, For Coagulation Tests, Stopper Siliconized Rubber With Protective Plastic Cover, Blue, Size 13X75 Mm. Labeled Tubes, Containing: Bare
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