THICKSTER

GUDID 00781311660229

disposable latex glove, powder-free, blue, medium, 50 pack

Bunzl USA Holdings LLC

Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00781311660229
• NIH Device Record Key: ce3ec268-9a9d-4cb9-898a-f1aa19d966b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THICKSTER
• Version Model Number: 6602-20
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00781311660229 [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: 2024-04-05
• Device Publish Date: 2024-03-28

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