ONE Vanish Hyperthin

GUDID 10726893111308

Lubricated Male Latex Condoms

GLOBAL PROTECTION CORP.

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• Primary Device ID: 10726893111308
• NIH Device Record Key: 14963221-3874-4404-9b90-c38dbd9d6779
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ONE Vanish Hyperthin
• Version Model Number: 111302
• Company DUNS: 364614362
• Company Name: GLOBAL PROTECTION CORP.
• Device Count: 12
• DM Exempt: true
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00726893111301 [Primary]
GS1	10726893111308 [Package]; Contains: 00726893111301; Package: Bundle of 3, 12 pack [3 Units]; In Commercial Distribution
GS1	20726893111305 [Package]; Package: 24 bundles of 3 [24 Units]; In Commercial Distribution
GS1	80726893111307 [Unit of Use]

FDA Product Code

• HIS: Condom
• QRZ: External Condom For Anal Intercourse Or Vaginal Intercourse

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: 2020-06-23
• Device Publish Date: 2020-06-15

On-Brand Devices [ONE Vanish Hyperthin]

• 20726893111954: Male Lubricated Latex Condoms
• 10726893111308: Lubricated Male Latex Condoms
• 80726893114674: Latex Lubricated Condoms