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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
E600 Cord, For Micromotor FDA UDI
Model / Reference
MT600CD FDA UDI
Description
E600 Cord, For Micromotor FDA UDI

Identifiers

Catalog Number
M600 FDA UDI
Primary DI / UDI-DI
00990010301757 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe 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

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Manufacturer

Manufacturer
Beyes Dental Canada Inc

Sources (1)

  • FDA UDI 945654cb-2f59-4fb4-9f99-674ff2e02a2b 34 fields · synced May 31, 2026