BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    iLab Polaris Multi-Modality Guidance System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025

    ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112991·CORNEAL TREPHINE BLADE16MM

    Navajo Tribal Utility Authority - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012780·Navajo Tribal Utility Authority - 18 Metal

    ANTERIOR CONDYLAR RET 90 DEG

    FDA UDI
    W.H. Holden, Inc.·D9282011780·

    LIPOSUCTION CANNULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0992011780·LIPOSUCTION CANNULA COBRA

    Liposuction Cannula

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896108073·Liposuction Cannula Cobra Style 250 X 4 Millime...

    SL-PLUS LATERALIZED STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CEDIA DAU 6-ACETYLMORPHINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ENDOTAK C TRANSVENOUS DEFIBRILLATION LEAD IS-1

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 28, 2019

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 10, 2011

    MULTI-LINK 8

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code MAF·August 11, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

    PROMUS ELEMENT ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 2, 2013

    UNKNOWN SHOULDER METAGLENE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code HSD·September 12, 2019

    PROLENE MESH 15X15CM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·January 3, 2019

    COREVALVE 26MM AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 28, 2016

    UNKNOWN SHOULDER METAGLENE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWS·September 9, 2019