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

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HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

INTELLIVUE INFO CENTER IX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 19, 2023

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 1, 2024

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 29, 2014

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 8, 2011

ANEURX

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 8, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

HEMOCCULT® ICT TEST DEVICE

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

UNKNOWN COOLSCULPTING® SYSTEM

FDA Adverse Event
Injury ·ALLERGAN PLEASANTON·Product code OOK·December 5, 2021