BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    PULMO-MIST COMPRESSOR MODEL # 4323

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RUSCH MILLER-ABBOTT TUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROXIMATE RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GAG·March 22, 2006

    ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 3.5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·June 16, 2006

    ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·June 13, 2006

    ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006

    ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·June 19, 2006

    ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006

    45MM ARTICING LNR CUTR/BLUE RLD

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 21, 2005

    ENDO LINEAR CUTTERS-ETS45MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·June 8, 2006

    ENDOPATH ETS-FLEX45 ARTICULATING ENDOSCOPIC LINEAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 15, 2006

    EVOLIS TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 16, 2012

    ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 2.5 MM -

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·October 21, 2005

    ETS 45 ENDO LINEAR CUTTER BL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·December 19, 2005

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 30, 2007

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 18, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 16, 2011

    Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020

    Stryker End Cap, Standard T2 Humerus ¿6 mm Catalog Number: 18300003S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020