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Vivid KoolWhite

FDA UDI

Class I (US FDA UDI)

by Pearson Dental Supplies, Inc.

Identity

Trade Name
Vivid KoolWhite FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Model / Reference
A19-0200 FDA UDI

Identifiers

Primary DI / UDI-DI
D724A1902001 FDA UDI
FDA Product Code
EEG FDA UDI
GMDN Term
Dental/surgical polymerization lamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6475 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Dental/surgical polymerization lamp

Vivid KoolWhite by Pearson Dental Supplies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/surgical polymerization lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1907c105-f23d-45bf-b4ea-5da60a6c7829 32 fields · synced May 30, 2026