10 results
·
34ms
·
Sources: EU EUDAMED, US FDA
SABOURAUD BHI AGAR
FDA 510(k)
FDA Class 1
·Microbiology
UniTip Catheter
FDA UDI
Unisensor AG·07640172972410·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971840·
VITROS IMMUNODIAGNOSTIC PRODUCTS MYOGLOBIN REAGENT PACK; CALIBRATORS; RANGE VERIFIERS
FDA 510(k)
FDA Class 2
·Immunology
POWEReam 1/4 Drive
FDA 510(k)
FDA Class 2
·Orthopedic
OMNIPOD 5 PODS
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·August 27, 2025
UNIVERSAL INSERTER/EXTRACTOR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWB·June 6, 2017
STIMULATOR 37021 RX1 EXTERNAL
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·May 27, 2014
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 15, 2012
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·September 9, 2010