DUREX Intense Sensation Condom

GUDID 40302340082448

Condom

RB Health (us) LLC

Basic male condom, Hevea-latex

• Primary Device ID: 40302340082448
• NIH Device Record Key: bf2b220f-3242-454c-b27e-7e0f5954fba8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUREX Intense Sensation Condom
• Version Model Number: Condom
• Company DUNS: 081049410
• Company Name: RB Health (us) LLC
• Device Count: 1000
• 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: true
• 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: +1(800)756-5488
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat

Device Identifiers

Device Issuing Agency	Device ID
GS1	00302340082440 [Primary]
GS1	40302340082448 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081886

FDA Product Code

• HIS: CONDOM

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: 2020-03-12
• Device Publish Date: 2020-03-04

On-Brand Devices [DUREX Intense Sensation Condom]

• 10302340096581: Condom
• 00023400824403: Condom
• 40302340082448: Condom
• 00302340096584: Condom