Bioemmalab

GUDID 00860012750504

4x4 Silicone Foam Dressing

NUTRIARTMIS INC

Wound-nonadherent dressing, absorbent, antimicrobial

• Primary Device ID: 00860012750504
• NIH Device Record Key: 65e1788a-5d78-4e05-94d6-7fd105d60d1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bioemmalab
• Version Model Number: 50504
• Company DUNS: 130589814
• Company Name: NUTRIARTMIS INC
• 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: true
• 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	00860012750504 [Primary]
GS1	00860012750566 [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: 2025-02-14
• Device Publish Date: 2025-02-06