11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Flush Syringe (Prefilled 0.9% normal saline solution)
FDA 510(k)
FDA Class 2
·General Hospital
BD BBL™ Taxo™ Differentiation Discs for Hippurate
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902317242·BD BBL™ Taxo™ Differentiation Discs for Hippurate
OsteoMed
FDA UDI
OSTEOMED LLC·00845694022224·FPS Calcaneal Distractor Small Bent
LOCKING SCREW, FULLY THREADED 5X45 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 30, 2009
Deltec
FDA UDI
ICU MEDICAL, INC.·00610586024125·
SYNTHES SMALL COBINATION CLAMP-MR SAFE
FDA 510(k)
FDA Class 2
·Orthopedic
PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
ACCU-CHEK RAPID D INFUSION SET
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code FPA·November 14, 2008
UNKNOWN DEPUY HEAD BALL
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code JDI·September 1, 2011
V SERIES MONITOR
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC·Product code MHX·July 12, 2013
Revogene, Catalog no. 610210. IVD test instrument
FDA Enforcement
Class II
·Ongoing·Meridian Bioscience Inc·August 3, 2022