18 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Bernafon
FDA UDI
Bernafon AG·05711584090336·ZERENA 3 MNR FW 3.0
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101094·HELVESTON "BIG BARBIE" RETRACTOR 9MM
MClass
FDA UDI
Conmed Corporation·10845854021040·MCLASS OSCILLATING SAW BLADE 19 X 1.27 (0.050")...
CONMED
FDA UDI
Conmed Corporation·10845854021453·OSCILLATING SAW BLADE 19 X 1.27 X 90 MM
ConMed Linvatec
FDA UDI
Provision·B504OMT190127900·
CONMED
FDA UDI
Conmed Corporation·10845854021446·OSCILLATING SAW BLADE 19 X 1.27 X 105 MM
MClass
FDA UDI
Conmed Corporation·10845854021033·MCLASS OSCILLATING SAW BLADE 19 X 1.27 (0.050")...
VIDAS® GDH
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code MCB·May 25, 2018
VIDAS® C. DIFFICILE GDH
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code MCB·May 1, 2018
METATARSAL DECOMPRESSION IMPLANT, MODEL 100
FDA 510(k)
FDA Class 2
·Orthopedic
ELI 230 ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
TENDRIL DX
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 11, 2014
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
INTERNAL PADDLES OPTION FOR DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·June 30, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·September 7, 2012
OSCILLATING SAW BLADE 19 X 1.27 X 105MM QTY 5
FDA Adverse Event
Injury
·CONMED LARGO·Product code GFA·April 5, 2023
Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
FDA Enforcement
Class II
·Terminated·Teleflex Medical·July 16, 2014