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KOMET Abrasive Instruments

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name
KOMET Abrasive Instruments FDA UDI
Generic Name
Dental-professional prophylaxis brush, single-use FDA UDI
Model / Reference
9686.204.040.A2 FDA UDI

Identifiers

Catalog Number
9686.204.040 FDA UDI
Primary DI / UDI-DI
E226021752A21 FDA UDI
FDA Product Code
EHL FDA UDI
GMDN Term
Dental-professional prophylaxis brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental-professional prophylaxis brush, single-use

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

Similar devices

Also classified as Dental-professional prophylaxis brush, single-use.

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 80667541-f55d-4524-95be-8e1196044e48 33 fields · synced May 30, 2026