Punch Biopsy Set

GUDID 05060745557301

BLINK MEDICAL LIMITED

General surgical procedure kit, non-medicated, single-use

• Primary Device ID: 05060745557301
• NIH Device Record Key: 83cfed4f-8f31-432a-9bec-346fae6cfa79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Punch Biopsy Set
• Version Model Number: 79-0010A
• Company DUNS: 738288096
• Company Name: BLINK 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	05060745557295 [Primary]
GS1	05060745557301 [Package]; Contains: 05060745557295; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• OJV: Single Use Instrument Tray
• PYB: Minor Surgical Procedures Tray

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: 2023-10-18
• Device Publish Date: 2023-10-10

On-Brand Devices [Punch Biopsy Set]

• 05060745555468: 79-0010
• 05060745557301: 79-0010A