BEUDAMED
    38 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 ×

    ALCO-SCREEN 02

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813865·GENUMEDI PRO SILVER SIZE VI

    ArgenZ Anterior 95x12 #2

    FDA UDI
    ARGEN CORPORATION, THE·D818121256·Dental porcelain/ceramic restoration kit

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383505772·Gutta Percha Points is used to root canal filin...

    Logical High Wall Liner

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215124519·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970423·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970393·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970416·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970409·

    Z3 GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERIS STEAM PI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CUSTOM PROXIMAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    CUSTOMER PROXIMAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 19, 2014

    SILICONE HANDLE/QUICK COUPLING W/ ROTATING CAP

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·January 28, 2025

    CUSTOM PROXIMAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code JWH·January 8, 2015

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 13, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 1, 2011

    CUSTOM DISTAL FEMORAL IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    UNK- NON- STANMORE HIP REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code KRO·June 25, 2015