9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NOVA 12 ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Unity
FDA UDI
DIOMEDICAL CO.,LTD.·08800113960336·Unity Sacroiliac Joint Fixation - Threaded Coun...
APTUS(R) DISTAL HUMERUS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GE LOGIQ A100 MP, MODEL 2272413
FDA 510(k)
FDA Class 2
·Radiology
TARGET ADAPTER T2 SCN
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 21, 2012
COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 2, 2010
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·January 13, 2013
INCEPTA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014
OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
FDA Enforcement
Class II
·Terminated·Philips Medical Systems Nederlands·July 4, 2018