Am-20 E Rm

FDA UDI

Class I (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name: AM-20 E RM FDA UDI
Generic Name: Dental surgical power tool motor, pneumatic FDA UDI
Device Name: Air Motor FDA UDI
Model / Reference: 30107000 FDA UDI
Description: Air Motor FDA UDI

Identifiers

Primary DI / UDI-DI: J021301070001 FDA UDI
FDA Product Code: EFB FDA UDI
GMDN Term: Dental surgical power tool motor, pneumatic 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

Yes

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, pneumatic

Am-20 E Rm by W & H Dentalwerk Bürmoos GmbH — 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: W & H Dentalwerk Bürmoos GmbH

Sources (1)

FDA UDI 0ec2e460-264d-4ea1-acdf-fbc697a1b28f 33 fields · synced May 30, 2026