20 results · 20ms · Sources: EU EUDAMED, US FDA

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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