BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    MYOSURE CONTROL UNIT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450194539·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197412766·TC Greenberg-Par Scissors curved...

    SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

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

    CONVERTORS SMS POLYOLEFIN GOWN

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

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 20, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 26, 2014

    BLAKE DRAIN

    FDA Adverse Event
    Death ·ETHICON·Product code KOG·June 10, 2011

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·December 23, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·March 23, 2017

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·October 24, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·February 20, 2019

    SAFETYGLIDE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 17, 2026

    Merit Medical Surgical Convenience Kits, Custom and SPPT, Merit Medical, South Jordan, UT 84065. Part numbers: K05-01767A, K05-01769, K05-01769A, K09-03843M, K09-03951M, K09-05894F, K09-08610, K10-00033Q, K10-00382M, K10-00685K, K10-00984F, K10-01531F, K10-01826D, K10-01826F, K10-02902B, K10-03080D, K10-03378C, K10-03397B, K10-03590A, K10-03590B, K10-03659D, K10-03659F, K10-03659G, K10-03689, K10-03907B, K12-01342D, K12-01444B, K12-01468, K12-01484A, K12-01487, K12-01490A, K12-01593, K12-01638, K12-01661, K12-01667, K12-01667A, K12-01964, K12-01968, K12-02098, SPPT-100/C, SPPT-5F-10C, SPPT-5F-10L/A, SPPT-5F-7/C, SPPT-5F-7L/A.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code LRO·August 15, 2007

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·October 29, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·August 3, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·September 7, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·April 30, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·April 14, 2017

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·June 14, 2018