Durma+ Medium Foam Dressing, 7" x 4.7"

GUDID 00840117342248

Sterile-R

Dynarex Corporation

Negative-pressure wound therapy system foam dressing, antimicrobial

• Primary Device ID: 00840117342248
• NIH Device Record Key: fec31989-d7d5-4ba5-a282-2b4d8964347e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Durma+ Medium Foam Dressing, 7" x 4.7"
• Version Model Number: 3127
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 1
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117342217 [Package]; Package: Case [10 Units]; In Commercial Distribution
GS1	00840117342248 [Primary]

FDA Product Code

• NAB: Gauze / Sponge,Nonresorbable For External Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-10
• Device Publish Date: 2025-06-02

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