FDA UDI Not in Commercial Distribution 🇺🇸 United States

UTAS

DI: 00857901006392 · Model: UTAS System Type-51 Pattern/Multifocal/RETeval · L K C TECHNOLOGIES, INC.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
UTAS
Primary DI
00857901006392
Version / Model
UTAS System Type-51 Pattern/Multifocal/RETeval
Company Name
L K C TECHNOLOGIES, INC.
Labeler DUNS
606234730
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-04
Public Version
2
Public Version Date
2023-12-01
Public Version Status
Update
Public Device Record Key
fbb1d215-7935-4f1d-9519-e29556bd4f1a
Distribution End Date
2023-11-29

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous
GWE Stimulator, Photic, Evoked Response
HLG Pupillometer, Ac-Powered

GMDN Terms

Code Name
11482 Electroretinograph
11460 Electroretinograph electrode

Identifiers

Type ID
Primary 00857901006392

Customer Contacts

Phone
301-840-1992