7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VISTA ANTIGEN BRUCELLA MELITENSIS
FDA 510(k)
FDA Class 2
·Microbiology
EnSite Velocity Cardiac Mapping System v5.2
FDA 510(k)
FDA Class 2
·Cardiovascular
ALLIGATOR CUP FORCEPS
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ARTICUL/EZE M 28MM +1.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code LPH·February 21, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 20, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·July 31, 2014
Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026