103 results · 35ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

BERCHTOLD SURGICAL TABLES

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH·Product code FQO·April 8, 2010

BERCHTOLD CORP, CHROMOPHARE SUGICAL LIGHTING

FDA Adverse Event
Injury ·BERCHTOLD CORP.·Product code FSY·August 13, 2010

OPERON

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH & CO. KG·Product code FWY·July 28, 2011

OPERON

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH & CO. KG·Product code FWY·July 28, 2011

OPERON

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH & CO. KG·Product code FQO·December 30, 2011

OPERON

FDA Adverse Event
Malfunction ·BERCHTOLD CORP.·Product code FQO·December 30, 2011

CHROMOPHARE

FDA Adverse Event
Malfunction ·BERCHTOLD CORP.·Product code FSY·August 30, 2012

OPERON

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH & CO. KG·Product code GDC·November 22, 2010

CHROMOPHARE

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FSY·October 19, 2012

CHROMOPHARE

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FSY·October 19, 2012

CHROMOPHARE

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FSY·December 30, 2011

CHROMOPHARE

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FSY·December 30, 2011

LIGHTHEAD F628 W/O CARDANIC

FDA Adverse Event
Malfunction ·BERCHTOLD GMBH & CO. KG·Product code FSY·May 4, 2016

CARDANIC FOR D650 AC 3-POLE

FDA Adverse Event
Malfunction ·BERCHTOLD CORP·Product code FSY·December 27, 2016

OPERON B810

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FQO·January 13, 2004

OPERON

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FQO·March 15, 2004

OPERON

FDA Adverse Event
Other ·BERCHTOLD CORP.·Product code FQO·March 3, 2004

TELETOM 363

FDA Adverse Event
Malfunction ·BERCHTOLD CORP.·Product code KMI·February 25, 2002

TELETOM 700 SERIES

FDA Adverse Event
Malfunction ·BERCHTOLD CORP.·Product code FQO·October 17, 2003

OPERON B810

FDA Adverse Event
Malfunction ·BERCHTOLD CORP.·Product code FQO·December 22, 2003