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MoguCera C

FDA UDI

Class II (US FDA UDI)

by S & S Scheftner GmbH

Identity

Trade Name
MoguCera C FDA UDI
Generic Name
Dental casting non-noble alloy FDA UDI
Device Name
Ingots, 1000g FDA UDI
Model / Reference
138000 FDA UDI
Description
Ingots, 1000g FDA UDI

Identifiers

Catalog Number
138000 FDA UDI
Primary DI / UDI-DI
04260207850938 FDA UDI
FDA Product Code
EJH FDA UDI
GMDN Term
Dental casting non-noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3710 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental casting non-noble alloy

MoguCera C by S & S Scheftner GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting non-noble alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9faf16b7-dfcb-4f31-b85e-a6060eb09c74 34 fields · synced May 30, 2026