8 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CUSHING BAYONET, INSULATED BIPOLAR FORCEP
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Stainless Steel Femoral Retrograde and Ankle Arthrodesis Nailing System
FDA UDI
ORTHOFIX SRL·18033509851247·REVISION LOCKING SCREW STERILE THREAD D 8 MM L...
PULSE RATE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
MULTICHEM (R) MAGNESIUM REAGENT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·January 29, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 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