Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030989301

FEI Number

3030989301

Entity Name

TRIMEDIKA LTD

City/State/Country

Belfast Mid Ulster, GB

Establishment Address

Whiterock Business Park, 739 Springfield Road, Belfast Mid Ulster BT12 7FP, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

TriMedika Ltd (Owner Number: 10090687)

Owner / Operator Contact Address

Whiterock Business Park, 739 Springfield Road, Belfast, GB-ANN BT127FP, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TriTemp

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SDV	Clinical Electronic Thermometer	General Hospital	Class 2	880.2910	2026-01-20

Official Correspondent

Marie Rooney

US Agent Details

Robert Duffy Business: Medical Device Post-production Services Inc Email: bob.duffy@mdpps-inc.com Phone: (858) 2318858

Related Public Records

Same Entity

TriMedika Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030989301. Last updated year: 2026. Please use registration number 3030989301 when referencing this establishment in official correspondence.