9 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CARDIO-CARD HOLTER ECG MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
P.F.C. SIGMA
FDA UDI
DEPUY (IRELAND)·10603295233244·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 4 ...
SALTO TALARIS TOTAL ANKLE PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
Withings Thermo (Model SCT01)
FDA 510(k)
FDA Class 2
·General Hospital
HUDSON ISIS SUBGLOTTIC SEC. ET TUBE
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·January 23, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 13, 2011
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 21, 2014
Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 4, 20.0 mm; Ref 96-0544.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005
Depuy P.F.C. E Knee System TC3 Tibial Insert, 4, 20.0mm, 75mm M/L, 51mm A/P, UHMWPE/Ti-6AI-4V, sterile; Product Code/REF 96-0544.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·September 27, 2007