7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RIWO DRIVE GENERATOR
FDA 510(k)
FDA Class 2
·Orthopedic
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984304·anteriors; shade B2; mould 93
ORTHO PATIENT CHAIR
FDA 510(k)
FDA Class 1
·Dental
DUPONT DIMENSION(R) TOBRAMLLYCIN(TOBR) METHOD
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MONOPOLAR CAUTERY INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·February 28, 2013
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·February 10, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 6, 2014