← Back to catalogue

Amadeo M-Uk1023

FDA UDI

Class II (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name
AMADEO M-UK1023 FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
medical surgical unit FDA UDI
Model / Reference
30387000 FDA UDI
Description
medical surgical unit FDA UDI

Identifiers

Primary DI / UDI-DI
J021303870001 FDA UDI
FDA Product Code
ERL FDA UDI
DZI FDA UDI
HWE FDA UDI
GEY FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 FDA UDI
872.4120 FDA UDI
878.4820 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

Yes

FDA UDI

Category: Surgical power tool system control unit, line-powered

Amadeo M-Uk1023 by W & H Dentalwerk Bürmoos GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, line-powered.

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 231cd3e1-7480-4770-b5e1-9ea53de43d67 33 fields · synced May 30, 2026