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CareMaster

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
CareMaster FDA UDI
Generic Name
Dental handpiece maintenance unit FDA UDI
Device Name
CareMaster B,2 E-type attachments, 1 HighSpeed Handpieces FDA UDI
Model / Reference
HPL2011 FDA UDI
Description
CareMaster B,2 E-type attachments, 1 HighSpeed Handpieces FDA UDI

Identifiers

Primary DI / UDI-DI
00837699000475 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Dental handpiece maintenance unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental handpiece maintenance unit

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

Similar devices

Also classified as Dental handpiece maintenance unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 62e3f01e-6a27-4fe9-9f42-b3712d15b5d5 33 fields · synced May 30, 2026