Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011216300

FEI Number

3011216300

Entity Name

TARMETEC OU

City/State/Country

Tartu Tartumaa, EE

Establishment Address

Ringtee 6, Tartu Tartumaa 50105, EE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Tarmetec OU (Owner Number: 10061123)

Owner / Operator Contact Address

Ringtee 6, Tartu, EE-78 50105, EE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ACCESSORY EQUIPMENT, CARDIOPULMONARY BYPASS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KRI	Accessory Equipment, Cardiopulmonary Bypass	Cardiovascular	Class 1	870.4200	2019-08-23

Official Correspondent

Kalev Nurm

US Agent Details

Emily Valerio Email: emily.valerio@getinge.com Phone: (862) 2215193

Related Public Records

Same Entity

Tarmetec OU

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 3011216300. Last updated year: 2026. Please use registration number 3011216300 when referencing this establishment in official correspondence.