BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    OLYMPUS AU2700 CLINICAL CHEMISTRY ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CUSTOMED

    FDA UDI
    CUSTOMED INC·M20890029822·ADJUSTABLE BESIDE RAILS

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746105258·BRACKET NARROW TWIN MAX BICUSPID 018 TQ=-7 A=0 ...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450309940·

    TRI-LOCK HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A100 AESTHETIC DIODE LASER

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

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 2, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

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

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

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

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

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

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

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

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

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

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 13, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 28, 2011

    HARMONIC SCALPEL CURVED SHEAR (EXACT CODE UNK)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·February 5, 2008

    VUELOCK PLATE, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

    FDA Enforcement
    Class II ·Ongoing·Ventana Medical Systems, Inc.·August 28, 2024