Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009774086

FEI Number

3009774086

Entity Name

IDOMAN TEORANTA

City/State/Country

Ballinrobe Mayo, IE

Establishment Address

Killateeaun, Tourmakeady, Ballinrobe Mayo F12C6H0, IE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Idoman Teoranta (Owner Number: 10094088)

Owner / Operator Contact Address

Killateeaun, Tourmakeady, Ballinrobe, IE-MO F12C6H0, IE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GTS DUAL RED TUBING SET GTS DUAL BLUE TUBING SET

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PIN	Kidney Perfusion Kit	Gastroenterology, Urology	Class 2	876.5880	2025-11-19

Official Correspondent

Eamonn Keegan

US Agent Details

John Bruens Business: Global Transplant Solutions Inc. Email: jbruens@1gtsinc.com Phone: (864) 5926311

Related Public Records

Same Entity

Idoman Teoranta

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 3009774086. Last updated year: 2026. Please use registration number 3009774086 when referencing this establishment in official correspondence.