BEUDAMED
    42 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    CONSENSUS REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SONTEC LEMPERT RONGEUR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896048034·SONTEC LEMPERT RONGEUR STRAIGHT TIP

    HS Stand. Burr, Ø1.8x70, 50k

    FDA UDI
    Bien-Air Surgery SA·07630055506832·

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100542801·IN-OVATION® C EURO 022/U4 UNIV -7T 0A

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532601·IN-OVATION® C Roncone 022/U5-5 L3-3 CS HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532001·IN-OVATION® C Base Rx 022 U5-5/L3-3

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100542071·IN-OVATION® C CCO 022/U4&5 -9T 0A

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532611·IN-OVATION® C Roncone 022/U5-5 L3-3 CS-BC HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532111·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS-BC HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532101·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS HK

    SYRINGE 10ML SALINE FILL CHINA SP

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·June 21, 2019

    10 ML BD POSIFLUSH NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·August 16, 2019

    SNN SYSTEM INCLUDING THE TOMOGUIDE OPTION

    FDA 510(k)
    FDA Class 2 ·Neurology

    PLAIN AND CHRONIC GUT ABSORBABLE SURGICAL SUTURES, USP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TOTAL ASR FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·May 8, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

    DUAL COOLER/HEATER

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTR·May 13, 2011

    ARNDT ENDOBRONCHIAL BLOCKER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code CBI·November 20, 2018

    ARNDT ENDOBRONCHIAL BLOCKER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code CBI·December 11, 2018

    ARNDT ENDOBRONCHIAL BLOCKER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code CBI·August 17, 2020