8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CCS-200 SPIROMETER
FDA 510(k)
FDA Class 2
·Anesthesiology
C-1890
FDA 510(k)
FDA Class 1
·Dental
WI-FI BODY SCALE
FDA 510(k)
FDA Class 2
·Cardiovascular
TARGETING ARM PROX. LAT. TIBIA LEFT
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·February 2, 2012
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 20, 2025
BACTISEAL CL EVD 1.9MM CTH SET
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC·Product code JXG·May 22, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014
PROTECTA DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NIK·June 14, 2011