Uline Wht 3 Mil Nitrile Glvs-XL

GUDID 30850015055219

ULINE, INC.

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

• Primary Device ID: 30850015055219
• NIH Device Record Key: 49606f97-792e-49b5-91de-b713e81aae03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uline Wht 3 Mil Nitrile Glvs-XL
• Version Model Number: S-21082-X
• Company DUNS: 039612668
• Company Name: ULINE, INC.
• Device Count: 200
• 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	00850015055256 [Unit of Use]
GS1	10850015055253 [Primary]
GS1	30850015055219 [Package]; Contains: 10850015055253; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170393

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: 2021-08-05
• Device Publish Date: 2021-07-28

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• 30850015055493 - ULINE BULLET EARPLUGS REFILL: 2024-05-21
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