BEUDAMED
    918 results · 38ms · 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.

    DAMAE MEDICAL

    Manufacturer
    🇫🇷 France·1 Basic UDI-DI·2 Devices

    DAMAE MEDICAL

    FDA registration
    DAMAE MEDICAL·1 product·🇫🇷 France

    deepLive

    FDA UDI
    DAMAE MEDICAL·03775000102715·deepLive is intended to be used as a non-invasi...

    deepLive™

    Device
    EU MDR · Eu Md Class 2a ·DAMAE MEDICAL·On the market·5 countries

    deepLive™

    Device
    EU MDR · Eu Md Class 2a ·DAMAE MEDICAL·On the market·14 countries

    deepLive

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·DAMAE MEDICAL·2 devices

    ANGIODRAPE PACK DAMAS 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

    FDA Enforcement
    Class II ·Terminated·Customed, Inc·September 9, 2015

    ANGIODRAPE PACK DAMAS 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

    FDA Recall
    Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code LRO·July 10, 2015

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·December 3, 2018

    V3 RING UNIVERSAL

    FDA Adverse Event
    Injury ·DENTSPLY (N.Z.) LIMITED·Product code DZN·April 7, 2017

    R SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 21, 2025

    FLEXI-DAM

    FDA Adverse Event
    Injury ·DENT4YOU AG.·Product code EIE·September 19, 2024

    MASTER PIN WITH THREAD

    FDA Adverse Event
    Injury ·HAGER & MEISINGER GMBH·Product code DZL·December 22, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 29, 2022

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 4, 2023

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 1, 2016

    C0R50, 12X130 KII BALLOON BLNT TIP 6/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·March 2, 2017

    BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·July 3, 2019

    X-SMART PLUS VERSION 0202

    FDA Adverse Event
    Injury ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EGS·November 18, 2024

    PERFIX PLUG

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·June 22, 2023