9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LAP DISCS
FDA 510(k)
FDA Class 1
·Microbiology
MICROMAX TROCAR OBTURATOR
FDA UDI
Biomet Orthopedics, LLC·00880304438668·
Sklar®
FDA UDI
SKLAR CORPORATION·10649111098086·SIMON CURETTE #1 6.8MM 9.25"
GC-BC-01, GC-BC-02, GC-BC-03 BICARBONATE DRY PACKS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI
FDA 510(k)
FDA Class 1
·Neurology
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 17, 2013
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 9, 2013
UNIVERSAL TORQUE LIMITING ATTACHMENT AXSOS AO FIT
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·November 10, 2010
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 1, 2014