DURAMAX S Silicone super absorbent dressing 66023133

GUDID 05000223500832

Super Absorbent Dressing 8 x 8in

SMITH & NEPHEW MEDICAL LIMITED

Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 05000223500832
• NIH Device Record Key: e31314ff-6c0f-4b1d-846f-b9a7aa946cb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DURAMAX S Silicone super absorbent dressing
• Version Model Number: 66023133
• Catalog Number: 66023133
• Company DUNS: 216344051
• Company Name: SMITH & NEPHEW MEDICAL LIMITED
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05000223500825 [Primary]
GS1	05000223500832 [Package]; Contains: 05000223500825; Package: Carton [10 Units]; In Commercial Distribution
GS1	05000223500849 [Package]; Package: Case [20 Units]; In Commercial Distribution

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: 2022-07-07
• Device Publish Date: 2022-06-29

On-Brand Devices [DURAMAX S Silicone super absorbent dressing]

• 05000223500894: Super Absorbent Dressing 8 x 16in
• 05000223500863: Super Absorbent Dressing 8 x 10in
• 05000223500832: Super Absorbent Dressing 8 x 8in
• 05000223500801: Super Absorbent Dressing 6 x 8in
• 05000223500771: Super Absorbent Dressing 4 x 4in