FDA UDI In Commercial Distribution 🇺🇸 United States

Final Fit

DI: 04987669101346 · Model: 1.13 · NIDEK CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Final Fit
Primary DI
04987669101346
Version / Model
1.13
Company Name
NIDEK CO.,LTD.
Labeler DUNS
690635461
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
193910a0-4f59-4867-b4e7-fd5fdd7a40b5

Device Description

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 Final Fit software performs a simulation of postoperative corneal shape and generates shot data using the imported data that was measured by the ARK-10000 and amounts of correction that are entered. The Final Fit software has two major functions: 1.Generating shot data to be used with the EC-5000 based on the measured data of the ARK-10000 2.Comparing postoperative data measured by ARK-10000 with the preoperative or target data (Simulated data just before generating shot data)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZS Excimer Laser System

GMDN Terms

Code Name
17702 Ophthalmic excimer laser system

Identifiers

Type ID
Primary 04987669101346

Customer Contacts