← Back to catalogue

Maxso

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
MAXSO FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, electric FDA UDI
Device Name
M600P (Portable),Portable System Control Unit with Digital Speed Display, Autoclavable Brushless Motor, Cord for Micromotor FDA UDI
Model / Reference
MT6001 FDA UDI
Description
M600P (Portable),Portable System Control Unit with Digital Speed Display, Autoclavable Brushless Motor, Cord for Micromotor FDA UDI

Identifiers

Primary DI / UDI-DI
00837699000529 FDA UDI
FDA Product Code
EBW FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental surgical power tool motorized handpiece/set, electric

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

Similar devices

Also classified as Dental surgical power tool motorized handpiece/set, electric.

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 e5082c5f-1e00-4b8d-b270-0f4cf0f42b52 33 fields · synced May 31, 2026