DURAFIBER Ag 20x30cm 66800573

GUDID 05000223467968

Absorbent, gelling, silver fibrous dressing

SMITH & NEPHEW MEDICAL LIMITED

Exudate-absorbent dressing, hydrophilic-gel, antimicrobial

• Primary Device ID: 05000223467968
• NIH Device Record Key: af162243-fc9b-4ac7-adfc-7e28cd1b3c5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DURAFIBER Ag 20x30cm
• Version Model Number: 66800573
• Catalog Number: 66800573
• Company DUNS: 216344051
• Company Name: SMITH & NEPHEW MEDICAL LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05000223467470 [Primary]
GS1	05000223467968 [Package]; Contains: 05000223467470; Package: Carton [5 Units]; In Commercial Distribution
GS1	05000223467975 [Package]; Package: Case [8 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161289

FDA Product Code

• FRO: Dressing, Wound, Drug

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-07-22
• Device Publish Date: 2020-09-18

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