Nu Flex

GUDID 20850058725615

Blue Nitrile Powder free exam gloves 3.5 mil size large

Direct Marketing USA LLC

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

• Primary Device ID: 20850058725615
• NIH Device Record Key: 07a75294-dfff-467d-ab1e-10147410698a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nu Flex
• Version Model Number: 4504003
• 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	00850058725673 [Primary]
GS1	20850058725615 [Package]; Contains: 00850058725673; 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: 2024-05-15
• Device Publish Date: 2024-05-07

On-Brand Devices [Nu Flex]

• 30850058725612: Blue Nitrile exam gloves powder free 3.5 mil size X-Large
• 20850058725615: Blue Nitrile Powder free exam gloves 3.5 mil size large
• 00850058725666: Blue Nitrile powder free exam glove 3.5 mil size med