BEUDAMED
    12 results · 21ms · 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 ×

    ANEROID TYPE BLOOD PRESSURE KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517499479·Archon Screw, Ø4.0x15mm SD Fixed

    PROXIMALE - 28 CM (11") SMALLBORE EXT SET W/6-PORT NANOCLAVE MANIFOLD, CHECK VA

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·August 25, 2020

    React 68 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ERBE VIO ESU, MODEL VIO 200 S

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

    JUVEDERM ULTRA PLUS/30HV (VOLUME UNKNOWN)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·April 21, 2014

    PROLIFT +M PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·October 10, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 19, 2015

    SUMMIT POR TAPER SZ4 STD OFF

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code LPH·May 8, 2012

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 8, 2012

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·May 8, 2012

    PINNACLE SECTOR II CUP 54MM

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWA·May 8, 2012