10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
NELLCOR PURITAN BENNETT, 840 VENTILATOR SYSTEM (MODEL 840)
FDA 510(k)
FDA Class 2
·Anesthesiology
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·June 29, 2017
artegral
FDA UDI
Merz Dental GmbH·D7091970460·anteriors; shade D4; mould UBS
SIGMA
FDA UDI
DEPUY (IRELAND)·10603295250609·SIGMA TIBIAL INSERT FIXED BEARING CURVED PLUS 4...
ALLEZ SPINE CROSS CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
Sorin Connect
FDA 510(k)
FDA Class 2
·Cardiovascular
TENDRIL SDX
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·February 20, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·January 18, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 31, 2014
SIGMA XLK CVD PLUS INS 4 8MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 16, 2025