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 calliper FDA UDI
Device Name: CASTROVIEJO Caliper, 0-20mm, 3 1/2" FDA UDI
Model / Reference: BR42-58307 FDA UDI
Description: CASTROVIEJO Caliper, 0-20mm, 3 1/2" FDA UDI

Identifiers

Catalog Number: BR42-58307 FDA UDI
Primary DI / UDI-DI: 00840183509958 FDA UDI
FDA Product Code: HOE FDA UDI
GMDN Term: Ophthalmic calliper 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic calliper

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Br Surgical Llc

Sources (1)

FDA UDI 4889405a-f61a-4b5d-88fc-2bbfa917fc47 35 fields · synced May 30, 2026