Moldex

FDA UDI

Class I (US FDA UDI)

by Angelus Industria de Produtos Odontologicos S A

Identity

Trade Name: MOLDEX FDA UDI
Generic Name: Dental impression tray, single-use FDA UDI
Device Name: Disposable partial tray for double impression and bite registration. FDA UDI
Model / Reference: MOLDEX Posterior FDA UDI
Description: Disposable partial tray for double impression and bite registration. FDA UDI

Identifiers

Catalog Number: 252 FDA UDI
Primary DI / UDI-DI: 07898078652527 FDA UDI
FDA Product Code: EHY FDA UDI
GMDN Term: Dental impression tray, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6880 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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

Yes

FDA UDI

Category: Dental impression tray, single-use

Moldex by Angelus Industria de Produtos Odontologicos S A — 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: Angelus Industria de Produtos Odontologicos S A

Sources (1)

FDA UDI a9a63a80-94c0-46f3-b89f-5e9d2c7a51b9 35 fields · synced May 31, 2026