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KOMET Dental Tungsten Carbide Burs

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name
KOMET Dental Tungsten Carbide Burs FDA UDI
Generic Name
Carbide dental bur, single-use FDA UDI
Model / Reference
H283SU.314.012.GS FDA UDI

Identifiers

Catalog Number
H283SU.314.012 FDA UDI
Primary DI / UDI-DI
E226100024091 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Carbide dental bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 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

Yes

FDA UDI

Category: Carbide dental bur, single-use

KOMET Dental Tungsten Carbide Burs by Gebr. Brasseler GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbide dental bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a7fee79-f034-43a5-9ee4-80817d7c439f 33 fields · synced May 31, 2026