← Back to catalogue

CareMaster

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
CareMaster FDA UDI
Generic Name
Surgical power tool maintenance unit FDA UDI
Device Name
Automatic Handpiece Maintenance, 2 Turbines & 1 E-Type, 110V-220V FDA UDI
Model / Reference
HPL2010 FDA UDI
Description
Automatic Handpiece Maintenance, 2 Turbines & 1 E-Type, 110V-220V FDA UDI

Identifiers

Primary DI / UDI-DI
00628504370353 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Surgical power tool 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

No

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: Surgical power tool 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 Surgical power tool maintenance unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d35651a0-3be1-4725-ad68-ee93849db36a 33 fields · synced May 30, 2026