BEUDAMED
    35 results · 34ms · 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 ×

    MICROTHERMX MICROWAVE ABLATION SYSTEM, MODELS MTX-180 OR MTX

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

    Bur PM2-70 80K steel Ø1.0 St

    FDA UDI
    Bien-Air Surgery SA·17630055512984·

    Oticon

    FDA UDI
    Oticon A/S·05707131165244·ACPR, ITE VC AP WL R BE ACTO PRO

    V.A.T.S. SLIDING SHAFT SATINSKY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921007860·V.A.T.S SLIDER SATINSKY CLAMP STRONGLY CURVED A...

    V.A.T.S. SLIDING SHAFT SATINSKY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896003453·V.A.T.S SLIDER SATINSKY CLAMP STRONGLY CURVED A...

    Medallion®

    FDA UDI
    Merit Medical Systems, Inc.·00884450023624·

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494463563·Endoscopic Kerrison Punch D 3.5mm, 90°, WL 150mm

    WhisperPak 5.0cmH2O CPAP Gamida, Case 10

    FDA UDI
    Respironics Novametrix, LLC·00884838075597·

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    ULNAR HEAD IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MYSONO U5 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 3, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 4, 2015

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·March 15, 2023

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 8, 2015

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 8, 2013

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·September 16, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 12, 2011

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013