154 results · 53ms · Sources: EU EUDAMED, US FDA

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70/100 HO LASER ND

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASERS·Product code GEX·September 9, 1997

COHERENT EXCELLASE 55

FDA Adverse Event
Injury ·COHERENT MEDICAL LASER, INC.·Product code GEX·March 15, 1994

ULTIMA SE

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code HQF·August 8, 1997

NOVUS 2000

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·August 8, 1997

NOVUS 2000 DUAL FIBER

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code HQF·September 19, 1997

VERSAPULSE C

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·August 22, 1997

VERSAPULSE AESTHETIC C

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·September 19, 1997

925

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·September 29, 1997

XL40+

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·June 5, 1997

ULTIMA SE

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code HQF·April 17, 1997

ULTRAPULSE 5000 117V

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·May 29, 1997

ULTRAPULSE

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·May 6, 1997

NOVUS 2000

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code GEX·June 2, 1997

ULTRA PULSE 5000 117V

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code GEX·April 25, 1997

ULTIMA SE

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GROUP·Product code HQF·December 15, 1996

ORAL PHARYNGEAL II DEL. KIT

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code GEX·December 24, 1996

ZEISS 30 SL-OMNI

FDA Adverse Event
Other ·COHERENT MEDICAL LASER GRP.·Product code HQF·December 27, 1996

INFRATOME

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code GEX·March 13, 1997

920

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code GEX·March 13, 1997

930

FDA Adverse Event
Malfunction ·COHERENT MEDICAL LASER GROUP·Product code HQB·February 13, 1997