BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    TRYPTIC SOY BROTH W/C02,CYSTEINE & 1%

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MGB Alert Internal Control Set IC2-48rxn

    FDA UDI
    Elitechgroup Mdx LLC·03661540951596·The MGB Alert Internal Control Set IC2 consists...

    ACUMED

    FDA UDI
    Acumed LLC·10806378042119·LE System Utility Tray

    MODIFICATON TO: PYRAMID +4 ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    URGOCELL AG, ANTIMICROBIAL WOUND DRESSING WITH SILVER

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNSPECIFIED BY THE COMPLAINANT

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code OTN·April 3, 2014

    PERMOBIL CHAIRMAN KOALA MINI-FLEX

    FDA Adverse Event
    Injury ·PERMOBIL, INC.·Product code INI·October 16, 2012

    EXACTAMIX EVA BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KPE·May 27, 2015

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021