9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DISPOSABLE HEAT AND MOSITURE EXCHANGER AND HME/FILTER
FDA 510(k)
FDA Class 1
·Anesthesiology
SONOPAK/QS, SONOPAK
FDA 510(k)
FDA Class 1
·Dental
MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28
FDA 510(k)
FDA Class 2
·Radiology
UNKNOWN DEPUY PFC SZ4 L FEMUR
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 30, 2010
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·February 6, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 21, 2014
BD SYRINGE ALLERGY 1ML W/NDL 27X1/2 RB
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 10, 2019
BD SYRINGE ALLERGY 1ML W/NDL 27X1/2 RB
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 10, 2019
BD PRECISIONGLIDE SYRINGE ALLERGY 1ML W/ NEEDLE 28X1/2 RB
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·May 31, 2019