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BR Surgical, LLC

FDA UDI

Class II (US FDA UDI)

by Br Surgical Llc

Identity

Trade Name
BR Surgical, LLC FDA UDI
Generic Name
General-purpose light source FDA UDI
Device Name
Replacement bulb for 250 watt BR900-225x-series Halogen Light Source FDA UDI
Model / Reference
BR900-5006 FDA UDI
Description
Replacement bulb for 250 watt BR900-225x-series Halogen Light Source FDA UDI

Identifiers

Catalog Number
BR900-5006 FDA UDI
Primary DI / UDI-DI
00840183528577 FDA UDI
FDA Product Code
FCW FDA UDI
GMDN Term
General-purpose light source FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose light source

BR Surgical, LLC by Br Surgical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose light source.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Br Surgical Llc

Sources (1)

  • FDA UDI 0e90256b-50d7-4d1e-ab53-35ec8f0f2758 35 fields · synced May 29, 2026