Bids Are Invited For Acquisition Of Materials And Equipment. For Dental, Veterinary And Laboratory Hospital Use (Collector, Cureation, Fio Etc), To Compose The Price Registration System.

Silicone Dressing, Minimum Specifications: Formed By A Layer Of Silicone On The Contact Surface, A Layer Of Soft Absorbent Polyurethane Foam Or Similar Technology And An External Film Impermeable To Water, Allowing Gas Exchange, Hypoallergenic, Flexible, With Soft Adhesion, Atraumatic Removal, Does Not Stick To Damp, Sterile, Disposable Single Use, Dimensions 7.5 X 7.5 Cm, Which May Vary By + Or Minus 1 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 Transfer With Aseptic Technique, Showing Externally Product Identification Data Batch Number Sterilization Validity Period Of At Least Two Years From The Date Of Sterilization Identification Data From The Manufacturer, Registration Number At The Ministry Of Health. Upon Delivery, The Product Must Have An Expiration Date Of At Least 12 Months, Set, For Pre-Operative Degermation, Based On Pvp With 1% Free Iodine, Consisting Of A Disposable Brush, With A Flexible Plastic Base And Polyurethane Sponge And Soft Bristles. Individual Packaging In Photosensitive Plastic Or In Rigid Blister, With A Lid In Laminated Paper Or Grade Paper Surgical, With Opening In Petala. Identification Data, Type Of Sterilization, Origin, Date Of Manufacture, Expiration Date And Registration With The Ministry Of Health Must Be Printed On The Packaging. Cylindrical ½ Circle (Can Vary Up To + 1Cm) For Gastrointestinal Surgery. Packaging That Guarantees The Integrity Of The Product Until The Moment Of 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, 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. Labeling: Primary And Secondary Packaging Labeled In Accordance With Rdc 185/01/Anvisa., 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 Anvisa/Ms. Registration, Collector, Examination, Universal Type, For Feces And Urine, Cup Type, Without Lubricant, Capacity Of 50 Ml, Graduated Up To 50Ml, In Pvc, Matte White Or Translucent, Lid With Screw Closure. You Must Present Anvisa Registration. Packaging Conditioned According To Current Regulations., 04/08/2026 - 18:30:18