DermaGinate

GUDID 00714196272485

DERMARITE INDUSTRIES LLC

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

• Primary Device ID: 00714196272485
• NIH Device Record Key: aac7f530-4e36-4ad6-bb78-508800b0374a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaGinate
• Version Model Number: 00272E
• Company DUNS: 883925562
• Company Name: DERMARITE INDUSTRIES LLC
• Device Count: 5
• 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	00714196272485 [Primary]
GS1	01714196535480 [Unit of Use]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

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 [DermaGinate ]

• 00714196275127: 00275E
• 00714196274120: 00274E
• 00714196272485: 00272E
• 00714196270443: 00270E
• 00714196260222: 00260E
• 00714196392060: 00275E
• 00714196392046: 00274E
• 00714196392008: 00272E
• 00714196391988: 00270E
• 00714196391964: 00260E