BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    DiLumen Endolumenal Interventional Scissors (DiLumen Is)

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

    ATRAMAT

    FDA UDI
    Internacional Farmacéutica, S.A. de C.V.·07500142068775·ATRAMAT SILK SURGICAL SUTURE BLACK USP 4-0 EP 1...

    ROCCIA

    FDA UDI
    Silony Medical GmbH·04054896028347·ROCCIA MultiLIF Cage 17x34 mm, 5° Lor.

    PRONTO V4 EXTRACTION CATHETER 5.5F; PRONTO V4 EXTRACTION CATHETER 6F; PRONTO V4 EXTRACTION 7F; PRONTO V4 EXTRACTION CATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLEXUR M

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·October 3, 2018

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 3, 2018

    NEOCIS GUIDANCE SYSTEM

    FDA Adverse Event
    Injury ·NEOCIS INC.·Product code PLV·September 13, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 10, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPB·June 17, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 23, 2011

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·May 19, 2024

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018