BEUDAMED
    9 results · 18ms · 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.

    HARGIS RECTAL SELF RETRATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PAQ.210X300X200/QT80/BDCK7985

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763009566·

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471155992·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 230mm

    OPTIMA NM/CT 640

    FDA 510(k)
    FDA Class 2 ·Radiology

    COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE

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

    DIACAM (510(K) K 901019)

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code KPS·March 13, 2001

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 17, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014