Uline Orange Nitrile Gloves - Powder-Free, Medium

GUDID 30850015055295

ULINE, INC.

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

• Primary Device ID: 30850015055295
• NIH Device Record Key: 8a104511-0167-4c95-95a2-765f60c7e606
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uline Orange Nitrile Gloves - Powder-Free, Medium
• Version Model Number: S-19251M
• 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	00850015055416 [Unit of Use]
GS1	10850015055413 [Primary]
GS1	30850015055295 [Package]; Contains: 10850015055413; 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: 2022-09-08
• Device Publish Date: 2022-08-31

Devices Manufactured by ULINE, INC.

• 30850015055509 - ULINE REUSABLE EARPLUGS - UNCORDED: 2024-08-02
• 30850015055516 - ULINE REUSABLE EARPLUGS - CORDED: 2024-08-02
• 30850015055523 - ULINE BULLET EARPLUGS - UNCORDED: 2024-07-31
• 30850015055530 - ULINE BULLET EARPLUGS - CORDED: 2024-07-31
• 30850015055547 - ULINE BELL EARPLUGS - UNCORDED: 2024-07-31
• 30850015055554 - ULINE BELL EARPLUGS - CORDED: 2024-07-31
• 30850015055493 - ULINE BULLET EARPLUGS REFILL: 2024-05-21
• 00850015055713 - ULINE EARPLUGS IN A BUCKET: 2024-05-21