Durma+ Transparent Wound Drape, 12" x 12"

GUDID 00840117342866

Sterile-EO

Dynarex Corporation

Synthetic polymer semi-permeable film dressing, adhesive

• Primary Device ID: 00840117342866
• NIH Device Record Key: f2050d32-a224-472c-afba-f8c9cd7e1914
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Durma+ Transparent Wound Drape, 12" x 12"
• Version Model Number: 3129
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117342842 [Package]; Contains: 00840117342859; Package: Case [20 Units]; In Commercial Distribution
GS1	00840117342859 [Package]; Package: Box [5 Units]; In Commercial Distribution
GS1	00840117342866 [Primary]

FDA Product Code

• KMK: Device, Intravascular Catheter Securement

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: 2025-06-11
• Device Publish Date: 2025-06-03

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