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KOMET Bur Blocks

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name
KOMET Bur Blocks FDA UDI
Generic Name
Sterilizer/disinfector rack instrument-holding insert, reusable FDA UDI
Model / Reference
9891.000. 3.A1 FDA UDI

Identifiers

Catalog Number
9891.000. 3 FDA UDI
Primary DI / UDI-DI
E226036292A11 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Sterilizer/disinfector rack instrument-holding insert, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Sterilizer/disinfector rack instrument-holding insert, reusable

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

Similar devices

Also classified as Sterilizer/disinfector rack instrument-holding insert, reusable.

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 e6604e64-f58d-452f-9be2-6f9dc89f4e81 33 fields · synced May 30, 2026