BEUDAMED
    22 results · 26ms · Sources: EU EUDAMED, US FDA

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    C.T.M. POWER CHAIR, MODEL HS-5600

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CUSTOMED

    FDA UDI
    CUSTOMED INC·M20890029832·MOTOR FOR SEMI ELECTRIC BED

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746105272·BRACKET NARROW TWIN MAX BICUSPID 022 TQ=-7 A=0 ...

    CERAMIX PORCELAIN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    LORENZ RESORBABLE DISTRACTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    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

    ANEURX ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 13, 2013

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·February 28, 2011

    CONTOUR CURVED CUTTER STAPLER

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

    Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP04

    FDA Enforcement
    Class II ·Ongoing·Integra LifeSciences Corp.·December 13, 2023

    UNKNOWN INITIAL PLACEMENT PRODUCT

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KGC·November 3, 2020

    VUELOCK PLATE, UNKNOWN SIZE

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