12 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRIMADO2 TOTAL SURGICAL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code HBC·March 26, 2018
SYRINGE 0.5ML 28GA 1/2IN BLS
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·February 25, 2021
MODULAR REPLACEMENT SYSTEM (MRS) HUMERAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
DK-PTCA BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
SYRINGE 0.5ML 28GA 1/2IN BLS 500CAS CA
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·April 5, 2021
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·October 1, 2014
NXSTAGE/SYSTEM ONE
FDA Adverse Event
Malfunction
·NXSTAGE MEDICAL·Product code KDI·November 13, 2008
ANCHORFAST ORAL ENDOTRACHEAL TUBE FASTENER
FDA Adverse Event
Malfunction
·HOLLISTER INCORPORATED·Product code CBH·May 29, 2013
SYRINGE 0.5ML 28GA 1/2IN
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·June 3, 2021
BD INSULIN SYRINGE WITH THE BD MICRO-FINE IV NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 9, 2021
BD INSULIN SYRINGE WITH THE BD MICRO-FINE IV NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·June 7, 2021