Guide Plug Collagen Wound Dressing

GUDID 04714691213682

MAXIGEN BIOTECH INC.

General oral wound dressing, animal-derived

• Primary Device ID: 04714691213682
• NIH Device Record Key: 1ae1320d-0708-48f9-b162-5bb0e73d5263
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Plug Collagen Wound Dressing
• Version Model Number: HAD001020
• Company DUNS: 657266016
• Company Name: MAXIGEN BIOTECH INC.
• Device Count: 10
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04714691213682 [Unit of Use]
GS1	04714691213705 [Primary]

FDA Product Code

• OLR: Oral Wound Dressing

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: 2025-03-21
• Device Publish Date: 2025-03-13

On-Brand Devices [Guide Plug Collagen Wound Dressing ]

• 04714691213699: HAD001520
• 04714691213682: HAD001020