45 results · 22ms · Sources: EU EUDAMED, US FDA

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IMPAX VOLUME VIEWING 3.0

FDA 510(k)
FDA Class 2 ·Radiology

NA

FDA UDI
MEDTRONIC XOMED, INC.·00681490034531·PROSTHESIS 1133135 CUP STAPES .6X4.0 SST

Per-Q-Cath Plus Midline Catheter

FDA UDI
Bard Access Systems, Inc.·00801741074868·Per-Q-Cath Plus Midline Catheter 3F Single-Lume...

STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

UNISTRIP 1

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

PULSE GEN MODEL UNK

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 6, 2022

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·June 30, 2022

NAIL, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code JDW·July 22, 2016

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·December 4, 2020

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVY·January 15, 2016

INCEPTA

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 15, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·July 22, 2016

BIPOL LEAD MODEL 300

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·August 21, 2008

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

ELECSYS 2010 RACK

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 26, 2009

PROTECTA XT CRT-D

FDA Adverse Event
Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·May 29, 2013

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 1, 2014

SPRINT QUATTRO SECURE

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·October 7, 2015

ARCHITECT C4000

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·April 30, 2024