6 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
OSTA MAXIGRO AND REGIGRO
FDA 510(k)
FDA Class 2
·Dental
Interphalangeal Joint Fusion Device Range
FDA 510(k)
FDA Class 2
·Orthopedic
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code FRN·January 31, 2014
ASR XL
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 26, 2010
CARESCAPE MONITOR B650
FDA Adverse Event
Malfunction
·GE HEALTHCARE FINLAND OY·Product code MHX·December 26, 2012