CABVI/High Five 72-10504R

GUDID 10610736274049

CABVI PF Cobalt Nitrile 72-1050xR SIZE XL, 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: 10610736274049
• NIH Device Record Key: e9fcce4a-999e-489d-9316-00f68ff988d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CABVI/High Five
• Version Model Number: 72-10504R
• Catalog Number: 72-10504R
• Company DUNS: 111267330
• Company Name: Ansell Healthcare Product
• Device Count: 1
• 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	00610736274042 [Primary]
GS1	10610736274049 [Package]; Contains: 00610736274042; 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: 2022-04-22
• Device Publish Date: 2022-04-14

On-Brand Devices [CABVI/High Five]

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• 10610736274032: CABVI PF Cobalt Nitrile 72-1050xR SIZE L, Nitrile Powder-Free Examination Glove
• 10610736274025: CABVI PF Cobalt Nitrile 72-1050xR SIZE M, Nitrile Powder-Free Examination Glove
• 10610736274018: CABVI PF Cobalt Nitrile 72-1050xR SIZE S, Nitrile Powder-Free Examination Glove
• 10071503216813: CABVI PF Cobalt Nitrile 72-1050xR SIZE XS, Nitrile Powder-Free Examination Glove