Kimono

GUDID 00850002174304

Kimono Microthin w Aqua Lube Latex Condom

LUNAMAX LLC

Basic male condom, Hevea-latex

• Primary Device ID: 00850002174304
• NIH Device Record Key: a7dff9f8-9e0d-4bb6-8b61-c63a92dabe71
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kimono
• Version Model Number: GS121
• Company DUNS: 106855461
• Company Name: LUNAMAX LLC
• Device Count: 1
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850002174304 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113686

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: 2018-12-31
• Device Publish Date: 2018-11-29

On-Brand Devices [Kimono]

• 00850002174335: Kimono Microthin Large Latex Condom
• 00850002174328: Kimono Microthin Large Latex Condom
• 00850002174311: Kimono Microthin w Aqua Lube Latex Condom
• 00850002174304: Kimono Microthin w Aqua Lube Latex Condom
• 00850002174298: Kimono Microthin Textured/Ribbed Latex Condom
• 00850002174281: Kimono Microthin Textured/Ribbed Latex Condom
• 00850002174182: Kimono Microthin Latex Condom
• 00850002174175: Kimono Microthin Latex Condom