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GoCheck Kids

FDA UDI

Class II (US FDA UDI)

by Gobiquity, Inc.

Identity

Trade Name
GoCheck Kids FDA UDI
Generic Name
Vision testing/training chart FDA UDI
Device Name
Mobile Application for Vision Screening FDA UDI
Model / Reference
Mobile Application Version 5.4.4 FDA UDI
Description
Mobile Application for Vision Screening FDA UDI

Identifiers

Primary DI / UDI-DI
B43050085440 FDA UDI
FDA Product Code
MMF FDA UDI
HOX FDA UDI
HKO FDA UDI
GMDN Term
Vision testing/training chart FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 FDA UDI
886.1150 FDA UDI
886.1760 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vision testing/training chartExternal ocular measurement camera

GoCheck Kids by Gobiquity, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External ocular measurement camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gobiquity, Inc.

Sources (1)

  • FDA UDI bd62599b-185e-4ada-888d-74bed862e285 33 fields · synced May 30, 2026