MICRO-TOUCH 313028060

GUDID 20076490616544

Micro-Touch Nitra-Free Blue 313028 Size XS, Nitrile Powder-Free Examination Glove

Ansell Healthcare Product

Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 20076490616544
• NIH Device Record Key: 038beb44-3024-4c0b-8a24-229cbc467a0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICRO-TOUCH
• Version Model Number: 313028060
• Catalog Number: 313028060
• Company DUNS: 111267330
• Company Name: Ansell Healthcare Product
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com
• Phone: 775-746-6600
• Email: jacob.ramirez@ansell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00071483002591 [Unit of Use]
GS1	10076490615687 [Primary]
GS1	20076490616544 [Package]; Contains: 10076490615687; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• LZA: Polymer Patient Examination Glove

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-04
• Device Publish Date: 2022-03-25

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