11 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Phoenix XL Dialysate Meter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028833·PESSARY, MARLAND #5, W/O SUPPORT, 3"
MONDEAL CONTOUR HO SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
V.A.C. ULTA NEGATIVE PRESSURE WOUND THERAPY SYSTEM (V.A.C. ULTA THERAPY SYSTEM) MODEL V.A.C. ULTA THERAPY UNIT MODEL U
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·August 28, 2019
SCREW AND PLATE HOLDING FORCEPS
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·April 15, 2020
SCREW AND PLATE HOLDING FORCEPS
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·February 14, 2020
BD 10ML SYRINGE LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 25, 2017
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
FENESTRATED BIPOLAR FORCEPSINSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 6, 2013
COLLEAGUE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011