8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
DXP1000 HOLTER RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
artegral life
FDA UDI
Merz Dental GmbH·D7091993618·anteriors; shade BL3; mould UBM
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690198406·AK3 PS Insert Trial Size 6, 18mm
ExactechGPS System
FDA 510(k)
FDA Class 2
·Neurology
BILI-MIRROR MODEL BLM-1
FDA 510(k)
FDA Class 2
·General Hospital
HOLDING SLEEVE-LONG FOR MATRIX
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code LXH·March 7, 2013
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 26, 2011
CAPSURE SP
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 8, 2014