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Hercules

FDA UDI

Class II (US FDA UDI)

by Aadco Medical, Inc.

Identity

Trade Name
Hercules FDA UDI
Generic Name
Mobile examination/treatment room light FDA UDI
Device Name
MOBILE LED EXAM & PROCEDURE LAMP OS-16 ARM 75000 LUX FDA UDI
Model / Reference
OS-716511LBP FDA UDI
Description
MOBILE LED EXAM & PROCEDURE LAMP OS-16 ARM 75000 LUX FDA UDI

Identifiers

Catalog Number
OS-716511LBP FDA UDI
Primary DI / UDI-DI
00840348502039 FDA UDI
FDA Product Code
FSY FDA UDI
GMDN Term
Mobile 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mobile 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 Mobile examination/treatment room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aadco Medical, Inc.

Sources (1)

  • FDA UDI 8334e41b-52a1-4bdb-838f-cbbb1b8fecf3 34 fields · synced May 30, 2026