Brasseler USA

FDA UDI

Class I (US FDA UDI)

by Peter Brasseler Holdings, LLC

Identity

Trade Name: Brasseler USA FDA UDI
Generic Name: Diamond dental bur, single-use FDA UDI
Device Name: BRIO6811.31.037 (C) BARREL 25P FDA UDI
Model / Reference: 5025900U0 FDA UDI
Description: BRIO6811.31.037 (C) BARREL 25P FDA UDI

Identifiers

Primary DI / UDI-DI: 00887919776994 FDA UDI
FDA Product Code: DZP FDA UDI
GMDN Term: Diamond dental bur, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4535 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Diamond dental bur, single-use

Brasseler USA by Peter Brasseler Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Peter Brasseler Holdings, LLC

Sources (1)

FDA UDI 33ac1c13-479a-4d13-8959-43ce15a08f32 33 fields · synced May 31, 2026