22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Weely Manual Wheelchair
FDA 510(k)
FDA Class 1
·Physical Medicine
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704509083·
MEDICAL MAGGOTS, LESOC
FDA 510(k)
FDA Unclassified
·Unknown
MODIFICATION TO MEDRAD 8-RECEIVER PHASED ARRAY NEUROVASCULAR COIL FOR SIEMENS
FDA 510(k)
FDA Class 2
·Radiology
BASIX COMPAK INFLATION SYRINGE KIT
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DTL·March 14, 2011
SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·June 4, 2019
PROX ACCESS 55MM ART STRP THI
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 8, 2013
NUVASIVE LATERAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code KWQ·June 27, 2011
PRECISION XTRA/OPTIUM
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 4, 2008
SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 1, 2024
14 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 26, 2024
SHIDEN
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 10, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
14 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 4, 2025
14 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 13, 2025
SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·April 18, 2022
SHIDEN
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 2, 2021
14 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·June 20, 2025
SHIDEN
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·January 6, 2022