Diva Condom

GUDID 80841445001216

Lubricated ultra thin condoms

GLOBAL PROTECTION CORP.

Basic male condom, Hevea-latex

• Primary Device ID: 80841445001216
• NIH Device Record Key: 1a44d458-7154-46b9-a811-73f106d5410f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Diva Condom
• Version Model Number: FGSW510201
• Company DUNS: 364614362
• Company Name: GLOBAL PROTECTION CORP.
• Device Count: 24
• 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

Customer Support Contacts

• Phone: 6129462800
• Email: ccataldo@globalprotection.com
• Phone: 6129462800
• Email: ccataldo@globalprotection.com
• Phone: 6129462800
• Email: ccataldo@globalprotection.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature in a dark, dry place. Avoid excessive heat.
• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature in a dark, dry place. Avoid excessive heat.
• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature in a dark, dry place. Avoid excessive heat.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841445001210 [Primary]
GS1	20841445000538 [Package]; Contains: 00841445001210; Package: case of 36 [36 Units]; In Commercial Distribution
GS1	80841445001216 [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: 2025-08-01
• Device Publish Date: 2025-07-24

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