BEUDAMED
    10 results · 20ms · 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 ×

    Plum Solo™ Precision IV Pump

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LCP

    FDA UDI
    Synthes GmbH·10886982168023·4.5MM LCP® PROXIMAL FEMUR PLATE 14 HOLES/355MM-...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295122845·TOTAL KNEE REV REAMER 14mm

    MDL SERIES DIODE LASERS, MODEL MDL-10/15

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

    Xia® Growth Rod Conversion Set

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 29, 2025

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD·Product code INM·November 11, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013