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Ceramill Sintron®

FDA UDI

Class II (US FDA UDI)

by Amann Girrbach AG

Identity

Trade Name
Ceramill Sintron® FDA UDI
Generic Name
Dental casting non-noble alloy FDA UDI
Model / Reference
Sintron R 71 XL (25mm) FDA UDI

Identifiers

Catalog Number
761107R FDA UDI
Primary DI / UDI-DI
E494761107R1 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental casting non-noble alloy

Ceramill Sintron® by Amann Girrbach AG — 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

Manufacturer
Amann Girrbach AG

Sources (1)

  • FDA UDI b44840aa-23c9-49b2-bdd4-546090a97164 34 fields · synced Jun 1, 2026