MYONE SAMPLER E88/51C

GUDID 80726893512791

2 Lubricated Latex Condoms

GLOBAL PROTECTION CORP.

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• Primary Device ID: 80726893512791
• NIH Device Record Key: 27094a3c-e6bc-4063-8419-ff53af7432b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MYONE SAMPLER E88/51C
• Version Model Number: MY-E88/51C-S02
• Company DUNS: 364614362
• Company Name: GLOBAL PROTECTION CORP.
• Device Count: 2
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00726893512795 [Primary]
GS1	80726893512791 [Unit of Use]

FDA Product Code

• HIS: Condom

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-11-07
• Device Publish Date: 2023-04-24

On-Brand Devices [MYONE SAMPLER E88/51C]

• 20726893512799: 2 Lubricated Latex Condoms
• 80726893512791: 2 Lubricated Latex Condoms