Meditech Kft

FDA Filings

This page includes the latest FDA filings for Meditech Kft. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3003764019
FEI Number3003764019
NameMEDITECH KFT.
Owner & OperatorMEDITECH KFT.
Contact Address24 Mikszath Kalman U --
BUDAPEST HU-NOTA 1184 HU
Official Correspondent
  • Zoltan - Csaba
  • 36-280-8232-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address24 Mikszath Kalman U
BUDAPEST Budapest, 1184 HU
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
MEDITECH KFT.
Model ABPM-052008-03-02
MEDITECH KFT.
Meditech Ambulatory Blood Pressure2008-03-02
MEDITECH KFT.
MEDITECH AMBULATORY BLOOD PRESSURE MONITOR, MODEL ABPM-052007-08-03
MEDITECH KFT.
MEDITECH MODEL ABPM-042005-11-18
MEDITECH KFT.
MEDITECH ABPM-04 AMBULA2003-01-29

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