20 results
·
20ms
·
Sources: EU EUDAMED, US FDA
NEUROMUSCULAR TRANSMISSION MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
Eclipse®
FDA UDI
Dentsply International Inc.·D0019050920·Original
VENTANA Anti MSH6 (SP93) Rabbit Monoclonal Primary Antibody
FDA UDI
Ventana Medical Systems, Inc.·07613336100578·For use with MMR IHC Panel
EchelonTM
FDA UDI
Micro Therapeutics, Inc.·00847536006317·190-5092-150 ECHELON14 90 PRESHAPE TIP
Echelon
FDA UDI
Micro Therapeutics, Inc.·00836462002371·14 Micro Catheter;90 Degree Tip Shape
SHARPLAN MODEL 1055 SEALED CO2 SURGICAL LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFIED SAFE VINYL EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ECHELON 14 MICROCATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC, INC. /MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR·Product code KRA·August 24, 2023
CONTACT DETACH
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 16, 2025
CONTACT DETACH
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 14, 2025
ECHELON MICRO CATHETER, MODELS 105-5092-150SA, 145-5092-150SA AND 190-5092-150SA AND SYRINGE ADAPTER ACCESSORY
FDA 510(k)
FDA Class 2
·Cardiovascular
HEMOLOK L CLIPS
FDA Adverse Event
Malfunction
·TELEFLEX·Product code FZP·May 27, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·January 9, 2013
COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 22, 2010
ECHELON
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code KRA·July 11, 2017
CONTACT DETACH
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 3, 2025
CONTACT DETACH
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 3, 2025
CONTACT DETACH
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 3, 2025
ECHELON
FDA Adverse Event
Malfunction
·MEDTRONIC DOMINICANA·Product code KRA·May 29, 2026
ECHELON
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code KRA·July 25, 2017