Jointown

GUDID 00810139473015

Disposable Nitrile Exam Glove Large Size 100/box, 10 boxes/case

U.S. HEALTH EXPRESS CORP.

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

• Primary Device ID: 00810139473015
• NIH Device Record Key: c9d31adc-daf7-4580-ad7a-21690bea462c
• Commercial Distribution Discontinuation: 2030-06-30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jointown
• Version Model Number: 2213
• Company DUNS: 081037169
• Company Name: U.S. HEALTH EXPRESS CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810139472049 [Primary]
GS1	00810139473015 [Package]; Contains: 00810139472049; Package: carton [10 Units]; Discontinued: 2030-06-30; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220693

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: 2025-05-14
• Device Publish Date: 2025-05-06

On-Brand Devices [Jointown]

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