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Forest

FDA UDI

Class I (US FDA UDI)

by Ls Enterprises, Inc.

Identity

Trade Name
Forest FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
OPERATORY LIGHT - HALOGEN, UNIT MOUNT, W/REMOTE TRANSFORMER, 110 VOLT, FOREST GREY FDA UDI
Model / Reference
9083G FDA UDI
Description
OPERATORY LIGHT - HALOGEN, UNIT MOUNT, W/REMOTE TRANSFORMER, 110 VOLT, FOREST GREY FDA UDI

Identifiers

Primary DI / UDI-DI
D0699083G0 FDA UDI
FDA Product Code
EAZ FDA UDI
GMDN Term
Operating room light 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating room light

Forest by Ls Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7f67c3f4-1929-48bb-9ffd-b169a9ce2597 33 fields · synced May 31, 2026