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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 power tool handpiece motorless component FDA UDI
Device Name
CS1-CH08, Contra Angle, Snap-On, 1:1 FDA UDI
Model / Reference
SL2033 FDA UDI
Description
CS1-CH08, Contra Angle, Snap-On, 1:1 FDA UDI

Identifiers

Primary DI / UDI-DI
00837699000697 FDA UDI
FDA Product Code
EGS FDA UDI
GMDN Term
Dental power tool handpiece motorless component 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool handpiece motorless component

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

Similar devices

Also classified as Dental power tool handpiece motorless component.

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 00490100-5209-42d3-b766-6deb0083fee6 33 fields · synced Jun 8, 2026