BEUDAMED
    12 results · 21ms · 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 ×

    ERGONOMIC PRODUCTS WORKSTATION

    FDA 510(k)
    FDA Class 1 ·Dental

    HHM

    FDA UDI
    Oticon A/S·05707131258373·H160, MINIRITE 312 WL SGR HHM

    DR COMFORT

    FDA UDI
    DJO, LLC·00888912235624·Sheer ThighHs OT W 20-30 BLK X

    PARELL NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896022034·PARELL NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED TIP

    IOP8 INTRA OPERATIVE PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    STAXX XDL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GENISTRONG

    FDA Adverse Event
    Malfunction ·GENICON·Product code GCJ·October 15, 2017

    INTERCHANGEABLE ULNAR ASSEMBLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019

    IROX

    FDA Adverse Event
    Malfunction ·GUIDANT ANGLETON/ST. PAUL·Product code DTB·October 1, 2014

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 29, 2013

    SYS 6 RECIP

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 11, 2011

    INTERCHANGEABLE HUMERAL ASSEMBLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019