← Back to catalogue

Medical Boom

FDA UDI

Class II (US FDA UDI)

by Amico Clinical Solutions Corp

Identity

Trade Name
Medical Boom FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
800mm 1000mm V-Series Arm (220A) - 1000mm 1000mm Normal Arm FDA UDI
Model / Reference
LP FDA UDI
Description
800mm 1000mm V-Series Arm (220A) - 1000mm 1000mm Normal Arm FDA UDI

Identifiers

Catalog Number
LP-8111-V-N-220A FDA UDI
Primary DI / UDI-DI
00684706009057 FDA UDI
FDA Product Code
FSY FDA UDI
GMDN Term
Operating 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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

Medical Boom by Amico Clinical Solutions Corp — Class II — 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

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

Manufacturer

Manufacturer
Amico Clinical Solutions Corp

Sources (1)

  • FDA UDI 96b1d4a0-b22a-47e2-8fc3-0f0de9b20308 36 fields · synced May 31, 2026