MyRx Visual Acuity

GUDID 07290018993408

6 OVER 6 VISION LTD

Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector

Primary Device ID	07290018993408
NIH Device Record Key	ee485092-6c12-4543-ae16-d0c791100dbb
Commercial Distribution Status	In Commercial Distribution
Brand Name	MyRx Visual Acuity
Version Model Number	1
Company DUNS	600351745
Company Name	6 OVER 6 VISION LTD
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	false
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	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290018993408 [Primary]

FDA Product Code

HOX	Chart, Visual Acuity
QTO	Digital Visual Acuity Test

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	2023-10-17
Device Publish Date	2023-08-30

On-Brand Devices [MyRx Visual Acuity ]

72900189934080	1
07290018993408	1