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Base metal alloy

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Base metal alloy FDA UDI
Generic Name
Dental bridge, metal-ceramic FDA UDI
Device Name
ticon Titanium primary crown FDA UDI
Model / Reference
Copings FDA UDI
Description
ticon Titanium primary crown FDA UDI

Identifiers

Catalog Number
010.2000 FDA UDI
Primary DI / UDI-DI
07630031703064 FDA UDI
FDA Product Code
EJH FDA UDI
GMDN Term
Dental bridge, metal-ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3710 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Base metal alloy by Institut Straumann 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

Sources (1)

  • FDA UDI 4dda39fd-efe3-494f-a85e-438a23fa6a8f 36 fields · synced May 30, 2026