9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MITAKA POINT SETTER
FDA 510(k)
FDA Class 2
·Neurology
11G BLADED MAMMOTOME ST PROBE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006
WVSM (Wireless Vital Signs Monitor) RWC + miniCap
FDA 510(k)
FDA Class 2
·Cardiovascular
PERFADEX AND PERFADEX WITH THAM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STERRAD 100S STERILIZER
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 7, 2013
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
INRATIO
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC·Product code GJS·February 7, 2011
STERRAD 100NX STERILIZER 1-DR
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 6, 2021