11 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FLOW-COUNT COULTER FLUOROSPHERES
FDA 510(k)
FDA Class 2
·Hematology
LEVEL ONE CMF
FDA UDI
KLS-Martin L.P.·00888118093769·PLATE, MINI, TLTS, STR, W/TAB, 17 MM BRG, 2.0-2...
STERILE DESIGN
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEARING AID, UNITRON MODEL VISTA 3000
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021
TBD
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·February 11, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 24, 2014
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 10, 2011
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
UNKNOWN
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022