Durma+ SiliGentle Silicone Foam Dressing, Bordered

GUDID 00840117345782

8" x 8" (20,3 cm x 20,3 cm), STERILE-EO

Dynarex Corporation

Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 00840117345782
• NIH Device Record Key: 1b426605-5b18-437b-8b09-5aa05d224559
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Durma+ SiliGentle Silicone Foam Dressing, Bordered
• Version Model Number: 3079
• 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	00840117345768 [Package]; Contains: 00840117345775; Package: Case [12 Units]; In Commercial Distribution
GS1	00840117345775 [Package]; Package: Box [10 Units]; In Commercial Distribution
GS1	00840117345782 [Primary]

FDA Product Code

• NAD: Dressing, Wound, Occlusive

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: 2025-12-18
• Device Publish Date: 2025-12-10

On-Brand Devices [Durma+ SiliGentle Silicone Foam Dressing, Bordered]

• 00840117345812: 8" x 6" (20,3 cm x 15,2 cm), STERILE-EO
• 00840117345782: 8" x 8" (20,3 cm x 20,3 cm), STERILE-EO
• 00840117345751: 4" x 8" (10,cm x 20,3 cm) , STERILE-EO