Medifoam

GUDID 08806129660178

Genewel Co.,Ltd.

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

• Primary Device ID: 08806129660178
• NIH Device Record Key: e17fc8e9-a72e-44ec-91c8-ffc6fae918b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medifoam
• Version Model Number: 12NJ05
• Company DUNS: 987669599
• Company Name: Genewel Co.,Ltd.
• Device Count: 10
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806129660178 [Unit of Use]
GS1	08806129660185 [Primary]

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: 2025-03-11
• Device Publish Date: 2025-03-03

On-Brand Devices [Medifoam]

• 08806129660093: Medifoam is indicated for the management of exuding wounds such as ulcers, burns, surgical/traum
• 08806129660178: 12NJ05