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Illuminix

FDA UDI

Class I (US FDA UDI)

by Illuminix Industries LLC

Identity

Trade Name
ILLUMINIX FDA UDI
Generic Name
Visual acuity projector FDA UDI
Device Name
Chart Visual Acuity FDA UDI
Model / Reference
SMART CHART FDA UDI
Description
Chart Visual Acuity FDA UDI

Identifiers

Primary DI / UDI-DI
00860010833285 FDA UDI
FDA Product Code
HOX 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

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: Visual acuity projector

Illuminix by Illuminix Industries LLC — 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

Sources (1)

  • FDA UDI 37039e34-1e7c-4218-a30d-19ca4366125c 34 fields · synced May 30, 2026