20 results · 23ms · Sources: EU EUDAMED, US FDA

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Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula

FDA 510(k)
FDA Class 2 ·Orthopedic

LEONE SPA

FDA UDI
LEONE SPA·08033707014294·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 11

Signature Femoral Head

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215001803·

MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT

FDA 510(k)
FDA Class 2 ·Cardiovascular

CARDIOFAX CE, MODEL ECG-1500 A

FDA 510(k)
FDA Class 2 ·Cardiovascular

ECOLAB

FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016

ECOLAB

FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016

ECOLAB

FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

WARMER DRAPE

FDA Adverse Event
Malfunction ·MICROTEK DOMINICANA, S.A.·Product code LHC·February 12, 2016

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·June 7, 2013

S-ICD SYSTEM

FDA Adverse Event
Injury ·CAMERON HEALTH·Product code LWS·August 11, 2014

UNK

FDA Adverse Event
Malfunction ·HOSPIRA, LTD.·Product code FPA·June 27, 2011

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·April 10, 2019

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code OLO·February 22, 2019

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code OLO·March 11, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·April 3, 2019