Final Fit™

GUDID 04987669100042

The Final Fit software receives the measured data from the Refractive Power/Corneal Analyzer OPD-Scan Model ARK-10000 via floppy disk etc. Then the Fi

NIDEK CO.,LTD.

Ophthalmic excimer laser system

• Primary Device ID: 04987669100042
• NIH Device Record Key: e44439b2-0973-497c-86b9-d399116cea86
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Final Fit™
• Version Model Number: 1.12
• Company DUNS: 690635461
• Company Name: NIDEK 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

Customer Support Contacts

• Phone: 1-800-223-9044
• Email: info@nidek.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987669100042 [Primary]

FDA Product Code

• LZS: Excimer Laser System

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-12-17

On-Brand Devices [Final Fit™]

• 04987669100042: The Final Fit software receives the measured data from the Refractive Power/Corneal Analyzer OPD
• 04987669100035: The Final Fit software receives the measured data from the Refractive Power/Corneal Analyzer OPD