7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APEX HOLE ELIMINATOR PS
FDA 510(k)
FDA Class 2
·Orthopedic
REFURBISH DIAGNOSTIC X-RAY EQUIPMENT
FDA 510(k)
FDA Class 2
·Radiology
TRU-CABLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PLM A+ PLATINUM MODU
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 19, 2014
PRISM HTLV-I/HTLV-II
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code MTP·February 15, 2013
X8000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·January 6, 2011
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026