Fisherbrand 19041171A

GUDID 20613647005082

Fisherbrand™ Comfort Nitrile Gloves 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: 20613647005082
• NIH Device Record Key: 93e938b5-ad2f-46a1-95d0-fd94a82e9fd9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fisherbrand
• Version Model Number: 19041171A
• Catalog Number: 19041171A
• Company DUNS: 111267330
• Company Name: Ansell Healthcare Product
• Device Count: 200
• 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	00613647005088 [Primary]
GS1	10613647005085 [Unit of Use]
GS1	20613647005082 [Package]; Contains: 00613647005088; 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: 2022-03-25
• Device Publish Date: 2022-03-17

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