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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
Surgical soft-tissue manipulation forceps, alligator, single-use FDA UDI
Device Name
HARTMAN-NOYES Alligator Ear Forcep, serrated, single-use, 3" , 10 per box FDA UDI
Model / Reference
BR98-26108 FDA UDI
Description
HARTMAN-NOYES Alligator Ear Forcep, serrated, single-use, 3" , 10 per box FDA UDI

Identifiers

Catalog Number
BR98-26108 FDA UDI
Primary DI / UDI-DI
00840183515881 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical soft-tissue manipulation forceps, alligator, single-use

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, alligator, single-use.

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 39ffc941-834a-48e3-90c8-d75e108c0034 35 fields · synced May 30, 2026