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Tri

FDA UDI

Class I (US FDA UDI)

by Tri Dental Implants Int. AG

Identity

Trade Name
TRI FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
A FDA UDI

Identifiers

Catalog Number
CS-3.3 FDA UDI
Primary DI / UDI-DI
07640149883244 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Tri by Tri Dental Implants Int. AG — Class I — 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
Tri Dental Implants Int. AG

Sources (1)

  • FDA UDI 5503c346-8cd3-4c5f-b272-98cfb8b4cc83 34 fields · synced Jun 1, 2026