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Vivid NuFill Unit Dose A3

FDA UDI

Class II (US FDA UDI)

by Pearson Dental Supplies, Inc.

Identity

Trade Name
Vivid NuFill Unit Dose A3 FDA UDI
Generic Name
Light-cured dental restorative composite resin FDA UDI
Device Name
20x .25g FDA UDI
Model / Reference
D010484 FDA UDI
Description
20x .25g FDA UDI

Identifiers

Primary DI / UDI-DI
D724D0104840 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Light-cured dental restorative composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Light-cured dental restorative composite resin

Vivid NuFill Unit Dose A3 by Pearson Dental Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light-cured dental restorative composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca9164f1-253f-4f4c-b2cf-f5a633a36e06 33 fields · synced Jun 1, 2026