7 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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3.0 ML RESERVOIR, MODEL 103/193
FDA 510(k)
FDA Class 2
·General Hospital
Arthrex®
FDA UDI
ARTHREX, INC.·00888867400894·1.9mm Snap-off FT Pin 36mm
BLADE ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
iNSitu Total Hip System
FDA 510(k)
FDA Class 2
·Orthopedic
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014