← Back to catalogue

Midwest®

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
MIDWEST® FDA UDI
Generic Name
Dental power tool non-rotary polishing endpiece FDA UDI
Device Name
MIDWEST® RDH Freedom® Cordless Prophy System - Lavender. Contains: 1 Basic System, 20 NUPRO Freedom® Disposable Prophy Angles, 1 Disposa-Shield® Trial Pack. FDA UDI
Model / Reference
90701L01 FDA UDI
Description
MIDWEST® RDH Freedom® Cordless Prophy System - Lavender. Contains: 1 Basic System, 20 NUPRO Freedom® Disposable Prophy Angles, 1 Disposa-Shield® Trial Pack. FDA UDI

Identifiers

Primary DI / UDI-DI
D00390701L011 FDA UDI
FDA Product Code
PEM FDA UDI
EKX FDA UDI
GMDN Term
Dental power tool non-rotary polishing endpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
872.4200 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

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

Midwest® by Dentsply Professional — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 5da8b3b7-316f-47fc-82bd-f7ba4ceee5ab 36 fields · synced Jun 8, 2026