Pontor MPF

FDA UDI

Class II (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name: Pontor MPF FDA UDI
Generic Name: Dental casting noble alloy FDA UDI
Device Name: Pontor MPF - 01050021 (31.1g) FDA UDI
Model / Reference: 01000297 FDA UDI
Description: Pontor MPF - 01050021 (31.1g) FDA UDI

Identifiers

Catalog Number: 01000297 FDA UDI
Primary DI / UDI-DI: 97640173081787 FDA UDI
FDA Product Code: EJT FDA UDI
GMDN Term: Dental casting noble alloy FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3060 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

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Weight — 31.1 Gram FDA UDI

Category: Dental casting noble alloy

Pontor MPF by Cendres+Métaux SA — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Cendres+Métaux SA

Sources (1)

FDA UDI f001e06b-2917-49ba-a7b5-0581c862a0e9 36 fields · synced May 30, 2026