DERMABOND PRINEO CLR222

GUDID 20705031237336

Skin Closure System, Liquid Adhesive

ETHICON, LLC

Wound closure set, topical

• Primary Device ID: 20705031237336
• NIH Device Record Key: 9c5275f4-41c7-4999-b32a-dd373930fcdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DERMABOND PRINEO
• Version Model Number: CLR222
• Catalog Number: CLR222
• Company DUNS: 829465157
• Company Name: ETHICON, 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705031237339 [Primary]
GS1	20705031237336 [Package]; Contains: 10705031237339; Package: BOX [2 Units]; In Commercial Distribution

FDA Product Code

• OMD: Cutaneous tissue adhesive with mesh

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-19
• Device Publish Date: 2016-09-01

On-Brand Devices [DERMABOND PRINEO]

• 20705031237336: Skin Closure System, Liquid Adhesive
• 10705031230996: Dermabond Prineo Skin Closure System
• 10705031024168: Dermabond Prineo Skin Closure System