DermaFilm thin with Border

GUDID 00714196229229

DERMARITE INDUSTRIES LLC

Exudate-absorbent dressing, non-gel, non-antimicrobial

• Primary Device ID: 00714196229229
• NIH Device Record Key: b336487d-efe8-4e9f-b819-4f5cf525f7e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaFilm thin with Border
• Version Model Number: 00229E
• Company DUNS: 883925562
• Company Name: DERMARITE INDUSTRIES LLC
• Device Count: 20
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00714196229229 [Primary]
GS1	01714196229228 [Unit of Use]

FDA Product Code

• NAD: Dressing, Wound, Occlusive

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-09
• Device Publish Date: 2020-09-01

On-Brand Devices [DermaFilm thin with Border]

• 00714196326706: 32670
• 00714196306661: 00306E
• 00714196259448: 00259E
• 00714196229229: 00229E
• 00714196391803: 32670
• 00714196391766: 00306E
• 00714196391742: 00259E
• 00714196391780: 00229E