23 results
·
112ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
8.3MHZ PENCIL PROBE 7 FOOT ODU CONNECTOR
FDA Adverse Event
Injury
·PARKS MEDICAL ELECTRONICS, INC.·Product code JOP·June 24, 2025
NA
FDA Adverse Event
PARKS MEDICAL ELECTRONICS, INC.·Product code IYN·August 31, 2015
FLOWMETER, BLOOD, CARDIOVASCULAR
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC.·Product code DPW·October 5, 2017
FLO-LAB
FDA Adverse Event
Injury
·PARKS MEDICAL ELECTRONICS INC.·Product code MHX·April 24, 2012
NA
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC.·Product code MHX·December 31, 2009
DOPPLER MODEL 812
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC.·Product code DPW·August 27, 2025
FLO LAB
FDA Adverse Event
Other
·PARKS MEDICAL ELECTRONICS, INC·Product code DXN·April 7, 2006
1052
FDA Adverse Event
Other
·PARKS MEDICAL ELECTRONICS, INC.·Product code IYN·April 10, 2006
9.1MHZ PENCIL PROBE
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC.·Product code JOP·June 2, 2025
FLO-LAB
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC.·Product code MWI·May 11, 2017
DOPPLER PENCIL PROBE
FDA Adverse Event
Malfunction
·PARKS MEDICAL ELECTRONICS, INC·Product code IYN·March 3, 2015
FLO-LAB
FDA Adverse Event
Other
·PARKS MEDICAL ELECTRONICS, INC. (PMEI)·Product code MHX·January 15, 2013
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 11, 2021
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 24, 2021
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·October 5, 2021
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 15, 2021
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 18, 2021
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code DTK·July 7, 2015
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 13, 2020
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 20, 2021