8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE
FDA 510(k)
FDA Class 1
·Anesthesiology
TriVerse X-Ray Digital Template, Tibial 40 MM Keel
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215114404·
ISE indirect K for Gen.2; ISE indirect Na for Gen.2; ISE indirect Cl for Gen.2; cobas pro integrated solutions
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PENUMBRA BALLOON GUIDE CATHETER, MODEL 7.5F
FDA 510(k)
FDA Class 2
·Cardiovascular
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 5, 2011
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·July 23, 2014
General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 General Pack, part number AMS5694
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017