← 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
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Silicone mat (for BR82-14001), 10 1/2" x 5" FDA UDI
Model / Reference
BR82-14085 FDA UDI
Description
Silicone mat (for BR82-14001), 10 1/2" x 5" FDA UDI

Identifiers

Catalog Number
BR82-14085 FDA UDI
Primary DI / UDI-DI
00840183521479 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Device sterilization/disinfection container, 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 Device sterilization/disinfection container, reusable.

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 376a2ed1-cac6-4ed9-b3a0-cd73e5a7f5a1 35 fields · synced May 31, 2026