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Midwest® E Pro

FDA UDI

Class I (US FDA UDI)

by Sirona Dental Systems GmbH

Identity

Trade Name
Midwest® E Pro FDA UDI
Generic Name
Dental power tool handpiece motorless component FDA UDI
Device Name
Midwest® E Pro PL 1:5 FDA UDI
Model / Reference
875185 FDA UDI
Description
Midwest® E Pro PL 1:5 FDA UDI

Identifiers

Primary DI / UDI-DI
E2768751850 FDA UDI
FDA Product Code
EFB 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool handpiece motorless component

Midwest® E Pro by Sirona Dental Systems GmbH — 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
Sirona Dental Systems GmbH

Sources (1)

  • FDA UDI f795add7-35b9-414e-9e37-738d84a945f8 34 fields · synced Jun 1, 2026