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EyeCheq Kiosk

FDA UDI

Class I (US FDA UDI)

by Eyecheq, Inc

Identity

Trade Name
EyeCheq Kiosk FDA UDI
Generic Name
Static ophthalmic equipment stand, electrically-adjusted FDA UDI
Device Name
Automated device stand designed to support, position, trigger, and retrieve results from ophthalmic diagnostic equipment during self-administered eye and health assessments in settings where clinical support is available if needed. FDA UDI
Model / Reference
A FDA UDI
Description
Automated device stand designed to support, position, trigger, and retrieve results from ophthalmic diagnostic equipment during self-administered eye and health assessments in settings where clinical support is available if needed. FDA UDI

Identifiers

Catalog Number
Q9063 FDA UDI
Primary DI / UDI-DI
G699Q90630 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Static ophthalmic equipment stand, electrically-adjusted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Static ophthalmic equipment stand, electrically-adjusted

EyeCheq Kiosk by Eyecheq, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Static ophthalmic equipment stand, electrically-adjusted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eyecheq, Inc

Sources (1)

  • FDA UDI fb0791d3-64fe-437e-a5e6-fd1ccf2be664 35 fields · synced May 31, 2026