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 ×

    AlignerFlow LC

    FDA 510(k)
    FDA Class 2 ·Dental

    MILAGRO

    FDA UDI
    Medos International Sàrl·10886705022250·MILAGRO ADVANCE INTERFERENCE SCREW Absorbable -...

    EXTRACORPOREAL SHOCK WAVE LITHOTRIPTER

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

    CELLPLEX TCP SYNTHETIC CANCELLOUS BONE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    S4 POLYAXIAL SCREW 6.0X35MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·October 15, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 1, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2013

    8X30MM MILAGRO ADVANCE INTERFERENCE SCREW

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HWC·October 16, 2017

    8X23MM MILAGRO ADVANCE INTERFERENCE SCREW

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MAI·October 16, 2017

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022