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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
SKEELE Chalazion Curette, round cup 1mm, serrated edge, 5" FDA UDI
Model / Reference
BR42-10373 FDA UDI
Description
SKEELE Chalazion Curette, round cup 1mm, serrated edge, 5" FDA UDI

Identifiers

Catalog Number
BR42-10373 FDA UDI
Primary DI / UDI-DI
00840183508111 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 7223d2aa-4e81-49fb-9d60-ab34c31b5c8d 35 fields · synced May 31, 2026