Cardiabase

FDA Filings

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

Cardiabase holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3007184699
FEI Number3007184699
NamePierre Wicker
Owner & OperatorCardiabase
Contact Address84 avenue du XXeme Corps
Nancy FR-54 Meurthe-et-Moselle 54000 FR
US Agent
Importing Logistics Registration
ImporterCardiabase
Address78 avenue du 20?me corps
Nancy, 54000 FRANCE
SubdivisionFR-54
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address30 High Street
Mystic, CT 06355 US
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
Pierre Wicker [Cardiabase]
Ambu2018-02-07
Pierre Wicker [Cardiabase]
3M2018-02-07
Pierre Wicker [Cardiabase]
Spacelabs 902072010-07-13
Pierre Wicker [Cardiabase]
Mortara H12+ Holter Recorder2010-04-22
Pierre Wicker [Cardiabase]
Mortara ELI-2502009-07-02
Pierre Wicker [Cardiabase]
Mortara ELI-1502009-07-01
Pierre Wicker [Cardiabase]
SpiderView (Ela Medical)2009-06-29

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