BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    RAPID IMF

    FDA 510(k)
    FDA Class 2 ·Dental

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481112614·LOCATOR R-Tx Abutment for 4.1mm External Hex Co...

    X-pedionTM

    FDA UDI
    Micro Therapeutics, Inc.·00847536004726·103-0605-200 XPEDION10 GWIRE 200CM ATH

    X-pedionTM

    FDA UDI
    Micro Therapeutics, Inc.·00847536004733·103-0605-200 XPEDION10 GWIRE 200CM ATH

    X-pedion

    FDA UDI
    Micro Therapeutics, Inc.·00836462003170·10 Hydrophilic Guidewire

    X-pedionTM

    FDA UDI
    Micro Therapeutics, Inc.·00847536004719·103-0605-200 X-PEDION 10

    X-Pedion

    FDA UDI
    Micro Therapeutics, Inc.·00763000518929·GUIDEWIRE 103-0605-200 V09 X-PEDION MDR

    X-Pedion

    FDA UDI
    Micro Therapeutics, Inc.·00763000294113·GUIDEWIRE 103-0605-200 V08 X-PEDION-10

    ATLAST DATA MANAGEMENT SOFTWARE (DMS)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    STACKHOUSE LENS HOOD, MODEL SA-700/F

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

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    ACCU-CHEK ® AVIVA

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·April 2, 2013

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 22, 2011

    COBAS 6000 E601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·April 16, 2008

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    ONYX AVM

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·April 15, 2026

    ECHELON

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code KRA·November 16, 2018

    ECHELON

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code KRA·November 16, 2018

    MARATHON

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·August 15, 2025

    RIST

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·January 28, 2025