7 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AIA-PACK PAP CALIBRATION VERIFICATION TEST SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
THUMPER
FDA 510(k)
FDA Class 2
·General Hospital
RUBEOLA IGG ELISA TEST
FDA 510(k)
FDA Class 1
·Microbiology
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH. LTD./ HUNTINGTON·Product code HQL·January 17, 2013
EON MINI IPG
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·December 9, 2010
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 10, 2014
ARROW CVC SET: 5-LUMEN 9.5FR X 20CM
FDA Adverse Event
Injury
·ARROW INTERNATIONAL LLC·Product code DQY·November 5, 2025