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Beyes

FDA UDI

Class II (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
Beyes FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
Anterior/Bite Wing Aiming Ring 1/PK FDA UDI
Model / Reference
DS1110 FDA UDI
Description
Anterior/Bite Wing Aiming Ring 1/PK FDA UDI

Identifiers

Primary DI / UDI-DI
00990010302471 FDA UDI
510(k) Number
K212279 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dental digital imaging sensor, intraoral

Beyes by Beyes Dental Canada Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9e0093e-bd07-4331-a874-612f477d0ea1 34 fields · synced May 30, 2026