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LuM

FDA UDI

Class I (US FDA UDI)

by Digital Doc LLC

Identity

Trade Name
LuM FDA UDI
Generic Name
LED dental light, battery-powered FDA UDI
Device Name
LUM Sub-Enamel Illumination FDA UDI
Model / Reference
LuM-1000 FDA UDI
Description
LUM Sub-Enamel Illumination FDA UDI

Identifiers

Catalog Number
LUM-1000 FDA UDI
Primary DI / UDI-DI
00813557020120 FDA UDI
FDA Product Code
EAZ FDA UDI
GMDN Term
LED dental light, battery-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4630 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: LED dental light, battery-powered

LuM by Digital Doc LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as LED dental light, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Digital Doc LLC

Sources (1)

  • FDA UDI 26e9cb06-e560-4637-828b-6dc564e8f019 34 fields · synced Jun 8, 2026