PRIMAPORE ADHESIVE WOUND DRSG 7.2*5CM 7133

GUDID 05000223071332

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: 05000223071332
• NIH Device Record Key: b56e5a39-db14-42da-8718-26ac80a1a05b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIMAPORE ADHESIVE WOUND DRSG 7.2*5CM
• Version Model Number: 7133
• Catalog Number: 7133
• 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	05000223071332 [Package]; Contains: 05000223415655; Package: Carton [100 Units]; In Commercial Distribution
GS1	05000223414931 [Package]; Package: Case [18 Units]; In Commercial Distribution
GS1	05000223415655 [Primary]

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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