FDA UDI In Commercial Distribution 🇺🇸 United States

MyRx Visual Acuity

DI: 07290018993408 · Model: 1 · 6 OVER 6 VISION LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyRx Visual Acuity
Primary DI
07290018993408
Version / Model
1
Company Name
6 OVER 6 VISION LTD
Labeler DUNS
600351745
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-30
Public Version
3
Public Version Date
2024-02-09
Public Version Status
Update
Public Device Record Key
ee485092-6c12-4543-ae16-d0c791100dbb

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QTO Digital Visual Acuity Test

GMDN Terms

Code Name
35922 Visual acuity projector

Identifiers

Type ID
Primary 07290018993408