8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AEROTEE, MODEL # 1001
FDA 510(k)
FDA Class 2
·Anesthesiology
TROCHANTERIC NAIL KIT, TI GAMMA3 11X200MM X 125
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 7, 2012
Single Use Electrosurgical Knife KD-625 , Single Use Electrosurgical Knife KD-645
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LEDEX, MODEL: WL-070
FDA 510(k)
FDA Class 2
·Dental
SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY
FDA Adverse Event
Injury
·Product code DTZ·September 11, 2007
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·February 28, 2013
UNICEL DXC 800 PRO SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·August 6, 2014
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 9, 2011