10 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PeDIA
FDA 510(k)
FDA Class 1
·Anesthesiology
TASMIN R 18°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844015025·The basic shape of the TASMIN R devices is a ho...
PHARMACARIBE INHALED SALINE SOLUTIONS
FDA 510(k)
FDA Class 2
·Anesthesiology
AFFIRM CO2 AND AFFIRM CO2 HP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DHS®/DCS® ONE-STEP LAG SCREW 12.7MM THREAD/95MM
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 17, 2014
LOFRIC HYDROKIT
FDA Adverse Event
Injury
·WELLSPECT HEALTHCARE·Product code GBM·June 14, 2013
EON MINI 16-CHANNEL RECHARGEABLE IPG
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, NEUROMODULATION·Product code LGW·July 6, 2011
BD BBL¿ TRYPTICASE¿ SOY AGAR WITH 5% SHEEP BLOOD (TSA II) // MACCONKEY II AGAR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·October 7, 2021
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 10, 2021
KIT BD MAX ENTERIC VIRAL PANEL
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code PCH·October 3, 2022