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BR Surgical, LLC

FDA UDI

Class I (US FDA UDI)

by Br Surgical Llc

Identity

Trade Name
BR Surgical, LLC FDA UDI
Generic Name
Cilia forceps FDA UDI
Device Name
BISHOP-HARMON Iris Forceps, straight, 1x2 teeth, 0.8mm tip, 3.5" FDA UDI
Model / Reference
BR42-94208 FDA UDI
Description
BISHOP-HARMON Iris Forceps, straight, 1x2 teeth, 0.8mm tip, 3.5" FDA UDI

Identifiers

Catalog Number
BR42-94208 FDA UDI
Primary DI / UDI-DI
00840183500030 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Cilia forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cilia forceps

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

Similar devices

Also classified as Cilia forceps.

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 e9abfd93-6499-40fa-bc18-5eb6efed7ac1 35 fields · synced Jun 1, 2026