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Nupro

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
Nupro FDA UDI
Generic Name
Cable/lead/sensor/probe cover, non-sterile FDA UDI
Device Name
Nupro Freedom™ with SmartMode™ Technology Cordless Prophy System Premium Kit - Lavender. Contains: 1 Cordless Prophy System, 3 Handpiece Sheaths, 200 Nupro Freedom® Disposable Prophy Angles, 500 Disposa-Shield® Barrier Trial Pack (Polyethylene Barriers) FDA UDI
Model / Reference
90741L03 FDA UDI
Description
Nupro Freedom™ with SmartMode™ Technology Cordless Prophy System Premium Kit - Lavender. Contains: 1 Cordless Prophy System, 3 Handpiece Sheaths, 200 Nupro Freedom® Disposable Prophy Angles, 500 Disposa-Shield® Barrier Trial Pack (Polyethylene Barriers) FDA UDI

Identifiers

Primary DI / UDI-DI
D00390741L031 FDA UDI
FDA Product Code
PEM FDA UDI
EKX FDA UDI
GMDN Term
Cable/lead/sensor/probe cover, non-sterile 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

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

Category: Dental polishing cup, single-useCable/lead/sensor/probe cover, non-sterile

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

Similar devices

Also classified as Cable/lead/sensor/probe cover, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0cb4c1b9-a190-47d6-942b-10dd9547cd2b 35 fields · synced May 31, 2026