ULINE BLACK EXAM NITRILE GLVS-M

GUDID 30850015055370

ULINE, INC.

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

• Primary Device ID: 30850015055370
• NIH Device Record Key: b4f4c3b7-20ab-4338-8a11-327a8f5e89bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULINE BLACK EXAM NITRILE GLVS-M
• Version Model Number: S-21081-M
• Company DUNS: 039612668
• Company Name: ULINE, INC.
• Device Count: 100
• 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: false
• 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	00850015055508 [Unit of Use]
GS1	10850015055505 [Primary]
GS1	30850015055370 [Package]; Contains: 10850015055505; 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: 2023-05-23
• Device Publish Date: 2023-05-15

On-Brand Devices [ULINE BLACK EXAM NITRILE GLVS-M]

• 30851253007138: Size Medium Gloves
• 30851253007978: Size Medium Gloves
• 30850015055370: S-21081-M