20 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TORNIER BIPOLAR RADIAL HEAD PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
ALPHA ORTHOPAEDICS AT3 SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PUMP-JECT SYRINGE WITH LUER-LOCK
FDA 510(k)
FDA Class 2
·General Hospital
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635876·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635869·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635913·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225190·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225213·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225251·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225237·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225244·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635883·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225220·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225206·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024225183·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635890·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024635906·
DUR OPT CER INS 32/52
FDA Adverse Event
Injury
·9616671 DEPUY (IRELAND)·Product code MRA·March 8, 2013
POLARIS DX¿ STEERABLE DIAGNOSTIC CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code DRF·February 16, 2011
HUDSON PEDIATRIC BREATHING CIRCUIT, 30"
FDA Adverse Event
Malfunction
·TELEFLEX·Product code OFP·July 24, 2014