MeniconZ (tisilfocon A) Blue

GUDID 00884465091014

MENICON CO.,LTD.

Rigid-gas-permeable corrective contact lens, extended-wear

• Primary Device ID: 00884465091014
• NIH Device Record Key: 5e5b04e2-4b04-46aa-a098-0c9effeb31f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MeniconZ (tisilfocon A) Blue
• Version Model Number: Blue
• Company DUNS: 690680533
• Company Name: MENICON CO.,LTD.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00884465091014 [Primary]

FDA Product Code

• MWL: Lens,Contact(Rigid Gas Permeable)-Extended Wear

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-20
• Device Publish Date: 2016-06-20

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• 00192538901017 - Deluxe Scleral Lens Kit: 2020-05-11
• 00192538901024 - Deluxe Kit: 2020-05-11
• 00192538901031 - Basic Scleral Lens Kit: 2020-05-11
• 00884465603064 - Miru 1day Menicon Flat Pack TC CP30: 2020-01-20