4 results
·
68ms
·
Sources: EU EUDAMED, US FDA
Ophthalmic Laser Diagnosis Device
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Suzhou Microclear Medical Instruments Co., Ltd·36 devices
ALLEGRETTO WAVE EYE-Q EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·July 12, 2018
ULTRAPULSE XL 3000/5000
FDA Adverse Event
Other
·LUMENIS LTD.·Product code GEX·April 2, 2007
EX-PRESS MINI GLAUCOMA SHUNT
FDA Adverse Event
Injury
·OPTONOL, LTD·Product code KYF·September 20, 2012