← Back to catalogue

TriniCHECK™ D-Dimer 1

FDA UDI

Class II (US FDA UDI)

by Tcoag Ireland Limited

Identity

Trade Name
TriniCHECK™ D-Dimer 1 FDA UDI
Generic Name
D-dimer IVD, control FDA UDI
Model / Reference
T4303 FDA UDI

Identifiers

Primary DI / UDI-DI
15391521420777 FDA UDI
510(k) Number
K003328 FDA UDI
FDA Product Code
GIZ FDA UDI
GMDN Term
D-dimer IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5425 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: D-dimer IVD, control

TriniCHECK™ D-Dimer 1 by Tcoag Ireland Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as D-dimer IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b046f221-2431-4822-88a1-b31abd468c8e 34 fields · synced Jun 1, 2026