16 results
·
53ms
·
Sources: EU EUDAMED, US FDA
MDSS GmbH
Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices
JETSTREAM G3
FDA Adverse Event
Injury
·PATHWAY MED TECHNOLOGIES, INC.·Product code MCW·December 29, 2010
SIMON NITINOL VENA CAVA FILTER
FDA Adverse Event
Injury
·NITINOL MED TECHNOLOGIES, INC.·Product code DTK·January 10, 1995
BIOJECTOR B2000
FDA Adverse Event
Other
·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 8, 2007
BIOJECTOR B2000
FDA Adverse Event
Other
·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 9, 2007
CALYPSO BEACON TRANSPONDERS
FDA Adverse Event
Injury
·CALYPSO MED TECHNOLOGIES INC·Product code IYE·January 12, 2010
SUBCLAVIAN CATHETER
FDA Adverse Event
Malfunction
·NEOSTAR MED TECHNOLOGIES, INC.·Product code LFJ·August 28, 1995
SAFETRACE TX
FDA Adverse Event
Malfunction
·GLOBAL MED TECHNOLOGIES, INC./WYNDGATE TECHNOLOGIES DIV·Product code MMH·October 11, 2001
SAFETRACE
FDA Adverse Event
Malfunction
·WYNDGATE TECHNOLOGIES / DIV GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·February 28, 2001
SAFETRACE
FDA Adverse Event
Malfunction
·WYNDGATE TECHNOLOGIES DIVISION/GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·July 22, 1999
SAFETRACE
FDA Adverse Event
Malfunction
·WYNDGATE TECHNOLOGIES DIVISION GLOBAL MED TECHNOLOGIES, INC·Product code MMH·March 8, 1999
Acorn Regulatory Consultancy Services Ltd
Authorized representative
🇮🇪 Ireland·16 Manufacturers·10848 Devices
MedNet EC-REP C III GmbH
Authorized representative
🇩🇪 Germany·12 Manufacturers·77 Devices
MedNet EC-REP GmbH
Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices
Advena Services Limited
Importer
🇲🇹 Malta·40 Manufacturers
Emergo Europe B.V.
Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices