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 ×

    Ranfac Cartilage Biopsy Needle

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LINK Instrument

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575180370·Trial Insert

    LINK Instrument

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575180363·Trial Insert

    LINK Instrument

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575180394·Trial Insert

    LINK Instrument

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575180387·Trial Insert

    ISOGRAY TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ASAHI REGALIA XS 1.0 PERIPHERAL GUIDE WIRE, MODELS PAGP 140000 & PAGP 1403000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    TOTAL ASR ACET IMP SIZE 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·June 21, 2013

    SEE H-10

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code HQL·October 17, 2014