BEUDAMED
    15 results · 20ms · 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 ×

    ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Screwdriver

    FDA UDI
    ADLER ORTHO SPA·08052693626854·POLIAXIAL SCREWDRIVER 416B HEX 3.5

    DURATWIX

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948032451·DURATWIX UNI, SIZE 10

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113003·PS Insert, Size 1 x 10mm

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707046026·STAINLESS STEEL LIGATURE WIRE .010

    VANGUARD SSK 360 LEFT FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 15, 2020

    VANGUARD SSK PSC FEMORAL STEM SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·December 4, 2019

    Sonoma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981086626·Cervical Awl

    Vital Signs™

    FDA UDI
    SUNMED, LLC·10889483057261·Vital Signs™ Anesthesia Circuit, 60" Pediatric ...

    ELEGANT NITRILE POWDER FREE EXAMINATION GLOVE BLUE VIOLET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO TRELEX MESH SURGICAL MESH

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

    Respan®

    FDA UDI
    SUNMED, LLC·10889483300275·Disposable Anesthesia Breathing Circuit, 60" Pe...

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·January 17, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·December 3, 2010

    COAGUCHEK® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·July 8, 2014