Beyes BR-1037

by Beyes Dental Canada Inc

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00990010302846 UDI-DI	Date8 Jun 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Beyes
Generic name: Carbide dental bur, reusable
Model / Ref / Catalog: BR-1037, 379/023-F

Primary DI / UDI-DI: 00990010302846
FDA product code: EJL
GMDN term: Carbide dental bur, reusable

Device class: Class I
Regulation number: 872.3240
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization
MRI safety: MR Safe

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Duray 3D Ceph

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See all devices from Beyes Dental Canada Inc →

Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number
Serial number
Manufacturing date

Other properties (9)

Supplied sterile: No
Single use: No
Implantable: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Expiration date: No