Needle, Neuro Stimulator, For Plexus Block, Dimension G22 Packaging That Allows Opening And Transferring 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., Glove, Surgical, Number 6, 5, Single Use, Non-Pyrogenic, In Natural Latex, Uniform Texture, Anatomical Shape, Traction Resistant, Cuff With Sheath, Minimum Length Of 265 Mm, And Minimum Width Of 76 Mm With Variation Of ± 6Mm, Minimum Thickness Of 0.10 Mm, Lubricated With Non-Toxic Bio-Absorbable Powder, With Right And Left Hand Indication, Non-Slip. Primary Packaging Individually Packed In Pairs, In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Aseptic, Sterile And Non-Pyrogenic Technique; The Primary Packaging Must Contain Identification Information And Characteristics Of The Product, Such As: Glove Size, Manufacturers Name, Date Of Manufacture, Sterilization Expiration Date; Secondary Packaging Must Comply With The Manufacturers Practice, In Order To Guarantee The Integrity Of The Product During Storage, 02/12/2025 - 18:31:33
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