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Nupro®

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
NUPRO® FDA UDI
Generic Name
Dental cavity varnish FDA UDI
Device Name
NUPRO® 5% Sodium Fluoride White Varnish, Patient Dose Kit - Raspberry. Contents: 50 Brush Applicators, Patient Doses of 0.25g, Prophy Cup Holder FDA UDI
Model / Reference
130227 FDA UDI
Description
NUPRO® 5% Sodium Fluoride White Varnish, Patient Dose Kit - Raspberry. Contents: 50 Brush Applicators, Patient Doses of 0.25g, Prophy Cup Holder FDA UDI

Identifiers

Primary DI / UDI-DI
D0031302271 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Dental cavity varnish FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 0.25 Gram FDA UDI

Category: Dental cavity varnish

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

Similar devices

Also classified as Dental cavity varnish.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f37c864a-2857-4850-bf44-49c856d0e3b1 36 fields · synced Jun 1, 2026