NuFlex

GUDID 00850058725475

Black Nitrile Powder Free Exam Gloves-Large (case) 1/10/100

Direct Marketing USA LLC

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

• Primary Device ID: 00850058725475
• NIH Device Record Key: 7263812d-0525-4604-b03a-cb94d7f6c279
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuFlex
• Version Model Number: 4504303
• Company DUNS: 079327950
• Company Name: Direct Marketing USA 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: true
• 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	00850058725468 [Primary]
GS1	00850058725475 [Package]; Contains: 00850058725468; Package: [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: 2023-12-06
• Device Publish Date: 2023-11-28

On-Brand Devices [NuFlex]

• 00850058725499: Black Nitrile Powder Free Exam gloves- X-Large (case) 1/10/100
• 00850058725475: Black Nitrile Powder Free Exam Gloves-Large (case) 1/10/100
• 00850058725451: Black Nitrile Powder Free Exam Gloves-Medium (case) 1/10/100
• 00850058725437: Black Nitrile Powder Free Exam Gloves-Small (Case) 1/10/100