7 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KOENIG TOTAL TOE IMPLANT
FDA 510(k)
FDA Unclassified
·Unknown
BARD URETEROSCOPIC CYTOLOGY BRUSH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BLADE, SCALPEL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
RECIPROC BLUE FILES, 6X, STERILE
FDA Adverse Event
Malfunction
·VDW GMBH·Product code EKS·December 8, 2025
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code BTI·June 19, 2014
UNK COONRAD/MORREY HUMERAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDC·October 19, 2010
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
MEDEL S.P.A.·Product code BTI·December 22, 2012