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TriniVerical™

FDA UDI

Class I (US FDA UDI)

by Tcoag Ireland Limited

Identity

Trade Name
TriniVerical™ FDA UDI
Generic Name
Multiple coagulation factor IVD, calibrator FDA UDI
Model / Reference
T5103 FDA UDI

Identifiers

Primary DI / UDI-DI
05391521420718 FDA UDI
FDA Product Code
DDF FDA UDI
GMDN Term
Multiple coagulation factor IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.5735 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple coagulation factor IVD, calibrator

TriniVerical™ by Tcoag Ireland Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple coagulation factor IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8fcb7169-fc26-49d1-b357-35fd963eed3d 33 fields · synced May 30, 2026