Speculum Leibinger

GUDID 05060480407626

BLINK MEDICAL LIMITED

Eyelid speculum, single-use

• Primary Device ID: 05060480407626
• NIH Device Record Key: c6a6d473-4779-4090-bfdd-7e2f6bf22aed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Speculum Leibinger
• Version Model Number: 31-3002
• 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	05060480402126 [Package]; Package: [10 Units]; In Commercial Distribution
GS1	05060480407626 [Primary]

FDA Product Code

• HNC: Specula, Ophthalmic

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: 2022-07-08
• Device Publish Date: 2022-06-30

On-Brand Devices [Speculum Leibinger]

• 05060480407626: 31-3002
• 05060480409538: 31-3002