Beyes

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name: Beyes FDA UDI
Generic Name: Carbide dental bur, reusable FDA UDI
Device Name: FG CARBIDE 332 FDA UDI
Model / Reference: 850051 FDA UDI
Description: FG CARBIDE 332 FDA UDI

Identifiers

Catalog Number: FG 332 FDA UDI
Primary DI / UDI-DI: 00990010300583 FDA UDI
FDA Product Code: EJL FDA UDI
GMDN Term: Carbide dental bur, reusable 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

FDA UDI

Single Use

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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Carbide dental bur, reusable

Beyes by Beyes Dental Canada Inc — 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: Beyes Dental Canada Inc

Sources (1)

FDA UDI 912a92bb-6378-46fc-a90d-a0a26c70093b 34 fields · synced May 30, 2026