50 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
INTERSTIM
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·August 29, 2008
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021
ULTRA-SELECT NITINOL GUIDEWIRE
FDA Adverse Event
Injury
·MICROVENA CORPORATION·Product code MKI·February 16, 1994
DGW .035 FC STR 150CM TEF LLT
FDA Adverse Event
Injury
·CORDIS CORP (MIAMI)·Product code MKI·June 7, 2000
CORDIS
FDA Adverse Event
Injury
·CORDIS ENDOVASCULAR·Product code MKI·June 7, 2000
DGW .035 MC J3MM 150CM TEF AMP
FDA Adverse Event
Injury
·CORDIS CORPORATION (MIAMI)·Product code MKI·June 29, 2005
BANDGRIP
FDA Adverse Event
Injury
·BANDGRIP INC.·Product code MKY·May 2, 2022
DERMACLOSE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·September 19, 2023
DGW .038 FC J3MM 150CM TEF
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code MKI·October 27, 2006
ARROW
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, INC.·Product code MKI·July 26, 1994
GUIDEWIRE FROM CV CATHETER KIT
FDA Adverse Event
Injury
·ABBOTT CRITICAL CARE SYSTEMS·Product code MKI·August 29, 1994
DERMACLOSE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 27, 2025
GLUIDEWIRE STANDARD .035
FDA Adverse Event
Injury
·TERUMO·Product code MKI·September 24, 1993
.016 GLIDEWIRE GOLD
FDA Adverse Event
Injury
·TERUMO·Product code MKI·July 27, 1993
.018 GLIDEWIRE ANGLED
FDA Adverse Event
Injury
·TERUMO·Product code MKI·July 27, 1993
.016 GLIDEWIRE GOLD
FDA Adverse Event
Injury
·TERUMO·Product code MKI·July 27, 1993
DERMACLOSE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 23, 2025