8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KSEA MODEL 203200 20 UNIMAT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690197058·Revision Knee Spiral Reamer- Hudson Short Flute...
CORUS-LX Implant
FDA 510(k)
FDA Unclassified
·Unknown
Zenysis Short-Term Dialysis Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ELECTRODE, PACEMAKER, PERMANENT
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
UNIFY CRT-D
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 23, 2014
COLLEAGUE CXE VOLUMETRICINFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 7, 2011
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026