Derma Tuff 66583

GUDID 10781311665832

disposable nitrile glove, powder-free, large, black, 120 pk

Bunzl USA Holdings LLC

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

• Primary Device ID: 10781311665832
• NIH Device Record Key: f4f23f28-021e-4ee1-846d-661a4dd7f2f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Derma Tuff
• Version Model Number: 66583
• Catalog Number: 66583
• Company DUNS: 799540588
• Company Name: Bunzl USA Holdings LLC
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10781311665832 [Primary]

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: 2022-10-31
• Device Publish Date: 2022-10-21

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