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MyRx Visual Acuity

FDA UDI

Class I (US FDA UDI)

by 6 Over 6 Vision Ltd

Identity

Trade Name
MyRx Visual Acuity FDA UDI
Generic Name
Visual acuity projector FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
07290018993408 FDA UDI
FDA Product Code
QTO FDA UDI
GMDN Term
Visual acuity projector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Visual acuity projector

MyRx Visual Acuity by 6 Over 6 Vision Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Visual acuity projector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
6 Over 6 Vision Ltd

Sources (1)

  • FDA UDI ee485092-6c12-4543-ae16-d0c791100dbb 32 fields · synced May 31, 2026