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PREMIOtitan

FDA UDI

Class II (US FDA UDI)

by Primotec Llc

Identity

Trade Name
PREMIOtitan FDA UDI
Generic Name
Dental casting non-noble alloy FDA UDI
Model / Reference
TI-13.5 FDA UDI

Identifiers

Primary DI / UDI-DI
D831TI135 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental casting non-noble alloy

PREMIOtitan by Primotec Llc — 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
Primotec Llc

Sources (1)

  • FDA UDI 973eb564-8ba2-4e29-bcf4-10cdb1fe1454 32 fields · synced May 30, 2026