48 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CELL SAVER ELITE
FDA 510(k)
FDA Class 2
·Anesthesiology
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564030856·Linen Pack I, Heart
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306819780·St Marks Retractor 7" With Lip Angled 15 degree
Suction Cup, ACD-CPR Device
FDA UDI
Zoll Medical Corporation·00847946028282·SUCTION CUP, ACD-CPR DEVICE
GOOD LUBRICATIONS
FDA 510(k)
FDA Class 1
·General Hospital
VENUS FREEZE SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·May 20, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 10, 2011
LIFEPAK CR PLUS DEFIRBILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·August 12, 2008
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code OKS·August 19, 2014
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·January 13, 2017
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·January 5, 2017
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016