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Demi Plus

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Demi Plus FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Device Name
LED Light Curing System 120V FDA UDI
Model / Reference
910860-1 FDA UDI
Description
LED Light Curing System 120V FDA UDI

Identifiers

Catalog Number
910860-1 FDA UDI
Primary DI / UDI-DI
00841396101656 FDA UDI
FDA Product Code
EBZ FDA UDI
GMDN Term
Dental/surgical polymerization lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6070 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

No

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/surgical polymerization lamp

Demi Plus by Kerr Corporation — Class II — 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

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 36471079-1586-47bf-8170-997ecf0ae272 36 fields · synced Jun 8, 2026