7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LISS BODY STIMULATOR MODEL SBL501-M
FDA 510(k)
FDA Class 2
·Neurology
SURGICAL FORCEPS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VASCULAR ACCESS PORT CONTINUOUS INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
LIBERTY CYCLER
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·June 13, 2014
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code MMI·November 10, 2010
ACCU-CHEK ULTRAFLEX
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·December 7, 2012
BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation.
FDA Enforcement
Class II
·Terminated·Stryker Sustainability Solutions·January 30, 2019