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

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    REDSENSE-ALARM UNIT AND SENSOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317300645·

    PMT CORPORATION - STEREOTACTIC

    FDA UDI
    PMT CORPORATION·00650551005254·DEPTHALON DEPTH ELECTRODE BONE STARTER

    POLOKOFF BONE RASPATORY

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896052475·POLOKOFF BONE RASPATORY DOUBLE ENDED SINGLE-SID...

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114223·LASIK CANNULA FLATTENED 25GA

    LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL), MODEL 621,622,623

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AMSCO HARMONY SURGICAL LIGHTING AND MEDIA SYSTEM

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

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+3MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·April 18, 2023

    VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 19, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·May 25, 2011

    KIT IMPLANTABLE SLIM TIP LEAD, 90CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·October 4, 2023

    PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·October 4, 2023

    VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022

    REVERSE SHOULDER SYSTEM 04.01.0173 GLENOSPHERE 39XØ27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·January 12, 2022

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·December 30, 2014

    UNK - SCREWS: 2.7 MM VA LOCKING

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·March 1, 2024