19 results · 54ms · Sources: EU EUDAMED, US FDA

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PNEUPAC FIRST RESPONDER WITHOUT ALARMS

FDA Adverse Event
Malfunction ·SMITHS MEDICAL PM, INC.·Product code BTL·June 26, 2009

NEURX DIAPHRAGM PACING SYSTEM

FDA Adverse Event
Death ·SYNAPSE BIOMEDICAL INC.·Product code OIR·May 3, 2016

DIALOG A + HE/BIC

FDA Adverse Event
Injury ·B. BRAUN AVITUM AG - MELSUNGEN·Product code FKJ·July 22, 2016

PNEUPAC PARAPAC WITHOUT ALARMS

FDA Adverse Event
Malfunction ·SMITHS MEDICAL PM, INC.·Product code BTL·May 23, 2009

KION

FDA Adverse Event
Injury ·MAQUET CRITICAL CARE AB·Product code BSZ·February 1, 2007

PNEUPAC PARAPAC WITHOUT ALARMS

FDA Adverse Event
Death ·SMITHS MEDICAL PM, INC.·Product code BTL·April 3, 2009

BEAR III

FDA Adverse Event
BEAR MEDICAL SYSTEMS INC.·Product code BTL·May 17, 1993

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023

DIALOG+®

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023

Wellkang Ltd

Authorized representative
259 Manufacturers·3500 Devices