Hercules

FDA UDI

Class II (US FDA UDI)

by Aadco Medical, Inc.

Identity

Trade Name: Hercules FDA UDI
Generic Name: Fixed examination/treatment room light FDA UDI
Device Name: ERGOLITE LAMP WITH ARM FDA UDI
Model / Reference: OS-511 FDA UDI
Description: ERGOLITE LAMP WITH ARM FDA UDI

Identifiers

Catalog Number: OS-511 FDA UDI
Primary DI / UDI-DI: 00840348501599 FDA UDI
FDA Product Code: FSY FDA UDI
GMDN Term: Fixed examination/treatment room light FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4580 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Fixed examination/treatment room light

Hercules by Aadco Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixed examination/treatment room light.

Chromophare F300 — Berchtold Holding GmbH · Class I
Celestial Star — Sunnex, Inc. · Class I
Celestial Star — Sunnex, Inc. · Class I
Tri Star — Sunnex, Inc. · Class I
Sim.LED 350 3p — S.I.M.E.O.N. Medical GmbH & Co. KG · Class I
MIRA Minor Surgery Light — Amico Lights Corporation · Class II
StarTrol — HUOT INSTRUMENTS, LLC · Class II
HexaLux — STERIS CORPORATION · Class I

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 II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Aadco Medical, Inc.

Sources (1)

FDA UDI b4b99277-4963-47ea-a017-bcbec3e7dc3f 34 fields · synced May 30, 2026