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Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
General/plastic surgery bur FDA UDI
Device Name
ST BUR BUD SHAPE COARSE MED (BUDBURMC) FDA UDI
Model / Reference
BUDBURMCST FDA UDI
Description
ST BUR BUD SHAPE COARSE MED (BUDBURMC) FDA UDI

Identifiers

Catalog Number
BUDBURMCST FDA UDI
Primary DI / UDI-DI
10653160282402 FDA UDI
FDA Product Code
GFF FDA UDI
GMDN Term
General/plastic surgery bur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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: General/plastic surgery bur

Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/plastic surgery bur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centurion Medical Products

Sources (1)

  • FDA UDI b483a220-06bb-4b63-a8f8-71c0ca0b029c 35 fields · synced Jun 1, 2026