Maxso S20A-IS

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name: Maxso S20A-IS FDA UDI
Generic Name: Dental laboratory drilling system handpiece FDA UDI
Device Name: S20A-IS, Straight Nose Cone, 1:1, Internal Spray, Non-Optic FDA UDI
Model / Reference: ST2008 FDA UDI
Description: S20A-IS, Straight Nose Cone, 1:1, Internal Spray, Non-Optic FDA UDI

Identifiers

Primary DI / UDI-DI: 00628504370704 FDA UDI
FDA Product Code: EFB FDA UDI
GMDN Term: Dental laboratory drilling system handpiece 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental laboratory drilling system handpiece

Maxso S20A-IS by Beyes Dental Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Beyes Dental Canada Inc

Sources (1)

FDA UDI 054ae3ae-c072-4090-86f0-8280eb43d624 33 fields · synced May 30, 2026