Medtronic Italia

FDA Filings

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

FDA Registration(s)
Registration Number3013242701
FEI Number3013242701
NameMEDTRONIC ITALIA
Owner & OperatorCovidien llc
Contact Address15 HAMPSHIRE STREET --
Mansfield MA 02048 US
Official Correspondent
  • Andrea Mitchell
  • x-508-2616327-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressVia Antica Tarsia 4
Rolo Reggio Emilia, 42047 IT
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
MEDTRONIC ITALIA [Covidien llc]
Anesthesia Breathing Circuit Kits2009-04-27
MEDTRONIC ITALIA [Covidien llc]
Flexlife2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hygrolife2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Airway Connector with Flex Tube2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Sterivent2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Sterivent S2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hygroster2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Barrierbac2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Barrierbac S2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Tracheolife2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hygroboy2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hygrobac2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hygrobaby2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Hybrobac S2008-02-15
MEDTRONIC ITALIA [Covidien llc]
Spirobac (& Adapters)2008-02-14
MEDTRONIC ITALIA [Covidien llc]
HME for Tracheostomized Patients1993-01-06

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