20 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula
FDA 510(k)
FDA Class 2
·Orthopedic
LEONE SPA
FDA UDI
LEONE SPA·08033707014294·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 11
Signature Femoral Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215001803·
MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIOFAX CE, MODEL ECG-1500 A
FDA 510(k)
FDA Class 2
·Cardiovascular
ECOLAB
FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016
ECOLAB
FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016
ECOLAB
FDA Adverse Event
ECOLAB·Product code LHC·January 21, 2016
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
WARMER DRAPE
FDA Adverse Event
Malfunction
·MICROTEK DOMINICANA, S.A.·Product code LHC·February 12, 2016
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·July 17, 2015
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·March 13, 2019
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 7, 2013
S-ICD SYSTEM
FDA Adverse Event
Injury
·CAMERON HEALTH·Product code LWS·August 11, 2014
UNK
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·June 27, 2011
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·April 10, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·February 22, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·March 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·April 3, 2019