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KOMET Dental Ceramic Burs

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name
KOMET Dental Ceramic Burs FDA UDI
Generic Name
Ceramic dental bur FDA UDI
Model / Reference
K1SM.204.027.A1 FDA UDI

Identifiers

Catalog Number
K1SM.204.027 FDA UDI
Primary DI / UDI-DI
E226041256A11 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Ceramic dental bur 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ceramic dental bur

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

Similar devices

Also classified as Ceramic dental bur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gebr. Brasseler GmbH & Co. KG

Sources (1)

  • FDA UDI 1cfe93c6-9299-4ab4-9f74-208793e410b9 33 fields · synced Jun 1, 2026