7 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MECTALIF POSTERIOR (TI PEEK) INTERBODY FUSION DEVICE PEEK/TI 9X22X12 L5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·December 18, 2020
MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·July 1, 2021
THERMAL SENSORY ANALYZER (TSA-II)
FDA Adverse Event
Injury
·MEDOC LTD., ADVANCED MEDICAL SURGERY MEDISCENSE USA·Product code LQW·December 26, 2019
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·January 18, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 14, 2014
QSENSE CPM THERMAL SENSORY ANALYZER 2001
FDA Adverse Event
Malfunction
·MEDOC LTD, ADVANCED MEDICAL SYSTEM·Product code LQW·April 19, 2022