← Back to catalogue

Mizzy

FDA UDI

Class I (US FDA UDI)

by Keystone Industries

Identity

Trade Name
Mizzy FDA UDI
Generic Name
Zinc oxide eugenol dental cement FDA UDI
Device Name
ZOE Cement Powder 21g FDA UDI
Model / Reference
6070500 FDA UDI
Description
ZOE Cement Powder 21g FDA UDI

Identifiers

Catalog Number
6070500 FDA UDI
Primary DI / UDI-DI
H66860705001 FDA UDI
FDA Product Code
EMB FDA UDI
GMDN Term
Zinc oxide eugenol dental cement FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3275 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Zinc oxide eugenol dental cement

Mizzy by Keystone Industries — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Zinc oxide eugenol dental cement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI 76e9ee5b-68e5-4a24-ac23-04e225da19ad 35 fields · synced Jun 9, 2026