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Cylindrical Straight Burr

FDA UDI

Class I (US FDA UDI)

by Brm Extremities

Identity

Trade Name
CYLINDRICAL STRAIGHT BURR FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Model / Reference
Ø2.0 X 20 mm - Stem lenght 60 mm FDA UDI

Identifiers

Catalog Number
BRB06S62020S FDA UDI
Primary DI / UDI-DI
08057717551266 FDA UDI
FDA Product Code
HTT FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Orthopaedic bur, single-use

Cylindrical Straight Burr by Brm Extremities — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Brm Extremities

Sources (1)

  • FDA UDI 6b5ef7b4-6a9b-412f-8e4a-3b78792060b7 35 fields · synced May 30, 2026