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Illuminix

FDA UDI

Class I (US FDA UDI)

by Illuminix Industries LLC

Identity

Trade Name
ILLUMINIX FDA UDI
Generic Name
Static ophthalmic equipment stand, manually-adjusted FDA UDI
Device Name
Stand for hold instruments for eye refraction examination FDA UDI
Model / Reference
ORBIT FDA UDI
Description
Stand for hold instruments for eye refraction examination FDA UDI

Identifiers

Primary DI / UDI-DI
00860010833223 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Static ophthalmic equipment stand, manually-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, manually-adjusted

Illuminix by Illuminix Industries LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Illuminix Industries LLC

Sources (1)

  • FDA UDI e945b60a-9bb3-43bc-ada9-2a97f288b716 34 fields · synced Jun 6, 2026