BEUDAMED
    346 results · 23ms · Sources: EU EUDAMED, US FDA

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    SACRAL STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·December 1, 2008

    SACRAL STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·December 1, 2008

    SACRAL STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·December 1, 2008

    AFFERA

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code QZI·July 11, 2025

    UNKNOWN_NEUWAVE

    FDA Adverse Event
    Injury ·NEUWAVE MEDICAL, INC.·Product code NEY·July 9, 2021

    CERAGLAZE PORCELAIN POLISHER (PRE-POLISH)

    FDA Adverse Event
    Injury ·AXIS DENTAL CORP.·Product code EHJ·October 15, 2008

    JIFFY POLISHER COARSE, DISK

    FDA Adverse Event
    Injury ·UNKNOWN·Product code EHJ·March 22, 2023

    POGO ONE STEP DIAMOND MICRO POLISHER

    FDA Adverse Event
    Injury ·DENTSPLY CAULK·Product code EHJ·April 8, 2004

    VENUS SUPRA

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER GMBH·Product code EHJ·September 17, 2013

    VENUS SUPRA

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER GMBH·Product code EHJ·September 17, 2013

    VENUS SUPRA

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER GMBH·Product code EHJ·November 12, 2013

    Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

    FDA Recall
    Open, Classified ·Ultradent Products, Inc.·Product code EHJ·January 28, 2026

    OptraPol Polishing Discs, Rx ONLY: OptraPol Refill Cup /10: REF/Product ID 634459, OptraPol Refill Small Flame/10: REF/Product ID 634458, OptraPol Assortment: REF/Product ID 634464 --Device Listing # B106952. One step polishing system for all common dental composites and amalgam.

    FDA Recall
    Terminated ·Ivoclar Vivadent, Inc.·Product code EHJ·July 11, 2016

    Disk, Abrasive

    FDA classification
    FDA Class 1 ·Disk, Abrasive

    CHJ

    FDA registration
    CHJ·3 products·🇯🇵 Japan

    HU-FRIEDY

    FDA UDI
    HU-FRIEDY MFG. CO., LLC·10889950009748·#5 Hourigan Elevator (Mod #38)

    KERECIS EHF

    FDA registration
    KERECIS EHF·4 products·🇮🇸 Iceland

    KERECIS EHF

    FDA registration
    KERECIS EHF·4 products·🇮🇸 Iceland

    KISO EHF

    FDA registration
    KISO EHF·1 product·🇮🇸 Iceland

    MyLab40 eHD

    FDA UDI
    Esaote Europe B.V.·08056304450388·