8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Medical Image Post-processing Software (uOmnispace.CT)
FDA 510(k)
FDA Class 2
·Radiology
AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Neuromaster G1 MEE200
FDA 510(k)
FDA Class 2
·Neurology
BD BBL¿ MUELLER HINTON II AGAR 150MM PLATE 24PK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 6, 2022
ARTICUL/EZE BALL 28+8.5 BL
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·November 20, 2008
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·July 23, 2013
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025