7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARABESK TOP
FDA 510(k)
FDA Class 2
·Dental
ACCUPROBE STREPTOCOCCUS PYOGENES CULTURE CONFIRM.
FDA 510(k)
FDA Class 1
·Microbiology
C.A.B. RING
FDA 510(k)
FDA Class 2
·Cardiovascular
MARATHON FLOW DIRECTED MICROC
FDA Adverse Event
Malfunction
·COVIDIEN·Product code KRA·March 1, 2013
IAB : 8 FR - 40 CC FOS
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC·Product code DSP·January 14, 2011
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·July 23, 2014
Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.
FDA Enforcement
Class II
·Terminated·Stryker Sustainability Solutions·July 1, 2015