6 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES (USA) UNIV SPINE ROD/SACRAL SCREW FIX SYST
FDA 510(k)
FDA Class 2
·Orthopedic
SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK
FDA 510(k)
FDA Class 1
·Ophthalmic
POWDER FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013
OT PING METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 16, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 12, 2014