Urease Test Used To Identification Of H. Pylori Bacteria In Gastric Mucosal Tissue (Biopsy) Collected By Endoscopy. Box Containing 50 Micro Tubes With 0.5 Ml Each (50 Tests)., Dressing, Hydrocolloid, Gel, With Pectin Carboxymethylcellose Sodium Water And Propylenol Glycol. Presentation Of A Tube Containing 15G. 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 From The Date Of Sterilization Identification Data Manufacturer, Registration Number At The Ministry Of Health. Upon Delivery, The Product Must Have An Expiration Date Of At Least 12 Months. Secondary Packaging Must Comply With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage Until The Moment Of Use. 3 Meters Long, Sterilized With Ethylene Oxide. Individual Packaging, In Surgical Grade Paper. The Packaging Must Be Printed With Identification Data, Origin, Date Of Manufacture, Type Of Sterilization, Expiration Date And Registration With The Ministry Of Health., Necklace, Cervical, Philadelphia Type, With Anterior Opening For Tracheostomy, Small, Polyform Or Softform Foam, With Chin Support, Provides Control Of Flexion/Extension And Rotation, Holes For Ventilation, Velcro Closure.Primary Packaging Individually Packaged In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of 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 ), Expiry Date, Composition, Instructions For Use, Warnings Or Precautions For Use, Name Of The Technical Person Responsible, Customer Service Number (Sac); The Secondary Packaging Must Be In Accordance With The Manufacturers Practice, Dilator Balloon For Achalasia, Low Compliance, With Radiopaque And Transparent Markers, Balloon With 30 Mm In Diameter And A Minimum Of 80 Mm In Extension, Catheter With A Minimum Of 90 Cm In Length. Sterile Product, Single Use. Individual Packaging In Surgical Grade Paper And Thermoplastic Film, Petala Opening. You Must Present Anvisa Registration. Individual Primary Packaging And Secondary Packaging Labeled According To Current Legislation., 03/05/2026 - 18:30:42, With Pectin Sodium Carboxymethylcellose Water And Propylenol Glycol. Presentation Of A Tube Containing 15G. Individually Packaged Packaging In Accordance With Rdc185/ Anvisa On Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Use, Registration Number With The Ministry Of Health. Upon Delivery, The Product Must Have An Expiration Date Of At Least 12 Months. Secondary Packaging Must Comply With The Manufacturers Practice