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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
Ophthalmic curette, reusable FDA UDI
Device Name
HEATH Chalazion Curette, one sharp and one blunt edge, size 3, 3mm, 4" FDA UDI
Model / Reference
BR42-10413 FDA UDI
Description
HEATH Chalazion Curette, one sharp and one blunt edge, size 3, 3mm, 4" FDA UDI

Identifiers

Catalog Number
BR42-10413 FDA UDI
Primary DI / UDI-DI
00840183513436 FDA UDI
FDA Product Code
HNZ FDA UDI
GMDN Term
Ophthalmic curette, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Ophthalmic curette, reusable

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

Similar devices

Also classified as Ophthalmic curette, reusable.

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 4a611543-df65-4100-b7ad-1809e3782383 35 fields · synced May 30, 2026