8 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TENS device-HeadaTerm 2 (Model: YF-HT2)
FDA 510(k)
FDA Class 2
·Neurology
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295116356·DELTA Xtend DELTA CTA HEAD REAMER
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295116349·DELTA Xtend DELTA CTA HEAD REAMING GUIDE
SEAMGUARD BIOABSORBABLE STAPLE LINE REINFORCEMENT MATERIAL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACCUMESH DEPLOYMENT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SOFTWARE CD-ROM CARELINK PRO EN
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code MDS·November 6, 2014
UNKNOWN NEXGEN KNEE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·August 23, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013