Nupro

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name: Nupro FDA UDI
Generic Name: Dental polishing cup, single-use FDA UDI
Device Name: NUPRO Freedom™ with SmartMode™ Technology Cordless Prophy System Basic Kit - Lavender - Contains: 1 Cordless Prophy System, 20 Nupro Freedom® Disposable Prophy Angles, 1 Disposa-Shield® Barrier Trial Pack (Polyethylene Barriers) FDA UDI
Model / Reference: 90741L01 FDA UDI
Description: NUPRO Freedom™ with SmartMode™ Technology Cordless Prophy System Basic Kit - Lavender - Contains: 1 Cordless Prophy System, 20 Nupro Freedom® Disposable Prophy Angles, 1 Disposa-Shield® Barrier Trial Pack (Polyethylene Barriers) FDA UDI

Identifiers

Primary DI / UDI-DI: D00390741L011 FDA UDI
FDA Product Code: PEM FDA UDI
EKX FDA UDI
GMDN Term: Dental polishing cup, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4370 FDA UDI
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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

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 polishing cup, single-use Cable/lead/sensor/probe cover, non-sterile

Nupro by Dentsply Professional — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Dentsply Professional

Sources (1)

FDA UDI a63117ca-90c4-4e6a-9e07-b583912d1a81 35 fields · synced Jun 6, 2026