50 results · 21ms · Sources: EU EUDAMED, US FDA

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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