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, 220V, POST MOUNT, W/ REMOTE FDA UDI
Model / Reference: 9083INT FDA UDI
Description: OPERATORY LIGHT, 220V, POST MOUNT, W/ REMOTE FDA UDI

Identifiers

Primary DI / UDI-DI: D0699083INT0 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ls Enterprises, Inc.

Sources (1)

FDA UDI c7301cd1-2d46-48fb-93ab-3202c335e88a 33 fields · synced Jun 1, 2026