BEUDAMED
    42 results · 31ms · 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 ×

    KING COBRA ANTERIOR CERVICAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERBRUGGE BONE CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896082519·VERBRUGGE BONE CLAMP WITH RATCHET RING HANDLE

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828158954·GEN4 INTERACTIVE

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828157391·GEN4 INTERACTIVE

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828164955·GEN4 INTERACTIVE

    Oph. Cystotomes

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113707·CYSTOTOME FORMED 23GA

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828114332·GEN4 INTERACTIVE

    SAVINA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIOSCANNER 2000

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Widex

    FDA UDI
    Widex A/S·05706069342185·WIDEX BABY440 BTE (Pearl white ) RC coil

    REMSTAR AUTO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR AUTO A-FLEX W/HUMID

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

    FDA Adverse Event
    Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 3, 2026

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,GER

    FDA Adverse Event
    Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

    CROSSCLIP

    FDA Adverse Event
    Malfunction ·CROSSROADS EXTREMITY SYSTEMS·Product code JDR·September 29, 2022

    V500, SAVINA AND VENTILATORS OF EVITA FAMILY

    FDA Adverse Event
    Other ·DRAGER MEDICAL GMBH·Product code CBK·February 18, 2011

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

    ASR ACETABULAR IMPLANT 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 9, 2013