9 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Peri-Guard and Supple Peri-Guard
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Drive Rail System
FDA UDI
ORTHOPEDIATRICS CORP.·00817867020634·CLAMP, 7-HOLE STACKED (5, 2)
GLOBAL CAP
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295104919·GLOBAL CAP HUMERAL HEAD TRIAL 52mm x 21mm
GLOBAL CAP
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295104902·GLOBAL CAP HUMERAL HEAD TRIAL 52mm x 18mm
ACUITY RADIATION THERAPY SIMULATOR
FDA 510(k)
FDA Class 2
·Radiology
Movement and Compressions System (the MAC System)
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·November 4, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 10, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 12, 2013