BEUDAMED
    13 results · 32ms · Sources: EU EUDAMED, US FDA

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    COMFOR-BOARD

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756379557·GYN LAPAROSCOPY PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112342·SURG-I-BAND ORANGE GLOW

    VALIDATE (R) GC3 CALIBRATION VERIFICATION / LINEARITY TEST KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NUMED HIGH PRESSURE PTA CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORTEX BLUSELECT TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 25, 2022

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 23, 2010

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 2, 2014

    5MM, 33CM PEEK MONOPOLAR HANDLE 33CM

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code KOG·December 3, 2012

    PORTEX BLUE LINE ULTRA SUCTIONAID

    FDA Adverse Event
    Injury ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·May 10, 2022

    PORTEX BLUE LINE ULTRA SUCTIONAID

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 18, 2022

    COMPRESS SHORT 5-HOLE DRILL GUIDE LARGE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code FZX·July 21, 2017

    TRACHEOSTOMY PVC - PORTEX TUBES BLUE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code BTO·October 13, 2022