10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REUSABLE PROBES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ReLine
FDA UDI
Nuvasive, Inc.·00195377072863·RELINE C Ti Rod, 3.5x70mm Pre Bent
LIQUID STABLE HBA1C CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Disposable Safety Self-destructive Syringes, 5 ML
FDA 510(k)
FDA Class 2
·General Hospital
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE HEALTH SOLUTIONS INC 00700006862·Product code LZG·January 18, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 30, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 17, 2014