BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    KT-1080/EE

    Device
    EU MDR · Eu Md Class 1 ·AGA Sanitätsartikel GmbH·On the market·32 countries

    LUX 1440

    FDA Adverse Event
    Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

    DV8 ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·MANUAL SURGICAL SCIENCES, LLC·Product code GAD·November 22, 2017

    STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON

    FDA Adverse Event
    Injury ·SPECTRANETICS·Product code ONU·July 12, 2019

    DV8 ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·MANUAL SURGICAL SCIENCES, LLC·Product code GAD·November 22, 2017

    DV8 ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·MANUAL SURGICAL SCIENCES, LLC·Product code GAD·November 22, 2017

    DV8 ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·MANUAL SURGICAL SCIENCES, LLC·Product code GAD·November 21, 2017

    SONENDO GENTLEWAVE SYSTEM

    FDA Adverse Event
    Injury ·SONENDO, INC.·Product code ELC·May 2, 2025

    DV8 ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·MANUAL SURGICAL SCIENCES·Product code GAD·January 8, 2018

    Kipptisch

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·AGA Sanitätsartikel GmbH·1 device