PRIMAPORE ADHESIVE WOUND DRSG 8.3*6CM 7135

GUDID 05000223071356

Non-woven adhesive wound dressing

SMITH & NEPHEW MEDICAL LIMITED

Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage

• Primary Device ID: 05000223071356
• NIH Device Record Key: 1d3dc12d-1cca-44b6-a48f-a3c41489f6ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIMAPORE ADHESIVE WOUND DRSG 8.3*6CM
• Version Model Number: 7135
• Catalog Number: 7135
• 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	05000223071356 [Package]; Contains: 05000223416751; Package: Carton [50 Units]; In Commercial Distribution
GS1	05000223416751 [Primary]
GS1	05000223416768 [Package]; Package: Case [12 Units]; In Commercial Distribution

FDA Product Code

• KGX: Tape And Bandage, Adhesive

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: 2020-07-16
• Device Publish Date: 2020-07-08

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