Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name: Henry Schein FDA UDI
Generic Name: Temporary dental filling material FDA UDI
Device Name: ZOE Temporary Cement FDA UDI
Model / Reference: 1011747 FDA UDI
Description: ZOE Temporary Cement FDA UDI

Identifiers

Catalog Number: 1011747 FDA UDI
Primary DI / UDI-DI: 00304040005101 FDA UDI
FDA Product Code: EMB FDA UDI
GMDN Term: Temporary dental filling material 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Weight — 45 Gram FDA UDI
Weight — 20 Gram FDA UDI

Category: Temporary dental filling material

Henry Schein by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Henry Schein, Inc.

Sources (1)

FDA UDI a62f06ef-85cf-4cb3-b627-7d9840062c14 36 fields · synced May 30, 2026