BEUDAMED
    21 results · 24ms · 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 ×

    LITHO DK30

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

    N/A

    FDA UDI
    TETRA MEDICAL SUPPLY CORP.·00614138122468·TETRA ULTRA ORTHO SHOE MALE LARGE

    Oticon

    FDA UDI
    Oticon A/S·05707131271365·NERA PRO, KIT 10 WL OMNI 75 BE

    SECONDARY TREPHINE

    FDA UDI
    Biomet Orthopedics, LLC·00887868004100·

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037282·Unitek(TM) Bicuspid Band General Purpose Wide L...

    NYOrtho APEX CORE Pommel Wheelchair Cushion Gel-Foam 14x14x3

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00810114601396·For patients requiring hip positioning, the NYO...

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857580985·Split Tube Retractor Ø12x50 mm

    ELI 250 ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ECLIPSE WITH AAA

    FDA 510(k)
    FDA Class 2 ·Radiology

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051414030RT10·#3 Toothed Cup, Parallel Bayonet, Right Facing STR

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051414031RT10·#3 Toothed Cup, Parallel Bayonet, Right Facing UP

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051414030LT10·#3 Toothed Cup, Parallel Bayonet, Left Facing STR

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051414031RT20·#3 Toothed Curette Bayonet Angled Up, Right Facing

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051414031LT10·#3 Toothed Cup, Parallel Bayonet, Left Facing UP

    PRONTO SPOT CHECK PULSE CO-OXIMETER

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·July 9, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    ACCU-CHEK CONFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 3, 2008

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 1, 2011

    MISONIX BONE SCALPEL TUBING SET MXB-T

    FDA Adverse Event
    Malfunction ·MISONIX INC.·Product code LFL·December 3, 2015

    INNOVA IGS 530

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS SCS·Product code OWB·August 2, 2019