Durasafe

GUDID 00640562123030

Vinyl powder free examination gloves 2303 medium

Durasafe Inc.

Vinyl examination/treatment glove, non-powdered

• Primary Device ID: 00640562123030
• NIH Device Record Key: 331ea1f1-1fa7-4290-8dfd-1b2c9fa0131d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Durasafe
• Version Model Number: 2303
• Company DUNS: 061046707
• Company Name: Durasafe 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00640562023033 [Primary]
GS1	00640562123030 [Package]; Contains: 00640562023033; Package: Case [10 Units]; In Commercial Distribution
GS1	10640562023030 [Unit of Use]

FDA Product Code

• LYZ: Vinyl 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: 2023-10-30
• Device Publish Date: 2023-10-20

On-Brand Devices [Durasafe]

• 00640562123054: Vinyl powder free examination gloves 2305 x-large
• 00640562023040: Vinyl powder free examination gloves 2304 large
• 00640562123030: Vinyl powder free examination gloves 2303 medium
• 00640562123023: Vinyl powder free examination gloves 2302, small