← Back to catalogue

BR Surgical, LLC

FDA UDI

Class I (US FDA UDI)

by Br Surgical Llc

Identity

Trade Name
BR Surgical, LLC FDA UDI
Generic Name
Ring cutter FDA UDI
Device Name
Finger Ring Cutter, 6-1/4" FDA UDI
Model / Reference
FG33-17300 FDA UDI
Description
Finger Ring Cutter, 6-1/4" FDA UDI

Identifiers

Catalog Number
FG33-17300 FDA UDI
Primary DI / UDI-DI
00840183502386 FDA UDI
FDA Product Code
FNS FDA UDI
GMDN Term
Ring cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6200 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: Ring cutter

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

Similar devices

Also classified as Ring cutter.

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
Br Surgical Llc

Sources (1)

  • FDA UDI 3cd1e397-a39e-44d5-804e-d68f469d3cd2 35 fields · synced Jun 6, 2026