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Cerapall 6

FDA UDI

Class II (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
Cerapall 6 FDA UDI
Generic Name
Dental casting noble alloy FDA UDI
Device Name
Cerapall 6 FDA UDI
Model / Reference
01050016_1OZ FDA UDI
Description
Cerapall 6 FDA UDI

Identifiers

Catalog Number
01050016 FDA UDI
Primary DI / UDI-DI
97640173080124 FDA UDI
FDA Product Code
EJS 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
Not 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Cerapall 6 by Cendres+Métaux SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cendres+Métaux SA

Sources (1)

  • FDA UDI 516ace99-cb9c-4d95-a28f-721203534865 36 fields · synced May 30, 2026