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Zone

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Zone FDA UDI
Generic Name
Fatty acid dental cement FDA UDI
Device Name
Zinc Oxide NonEugenol Temporary Cement Dual Barrel Syringe FDA UDI
Model / Reference
27043DX FDA UDI
Description
Zinc Oxide NonEugenol Temporary Cement Dual Barrel Syringe FDA UDI

Identifiers

Primary DI / UDI-DI
00814978024360 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Fatty acid dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

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 — 15 Gram FDA UDI

Category: Fatty acid dental cement

Zone by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fatty acid dental cement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 4531e4a6-5e35-46fd-8a84-4698c5690ae3 36 fields · synced Jun 8, 2026