BEUDAMED
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    IRP MEDICAL

    FDA registration
    IRP MEDICAL·1 product·🇺🇸 United States

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·October 26, 2022

    INNOVA 3100-IQ

    FDA Adverse Event
    Other ·GE MEDICAL SYSTEMS SCS·Product code OWB·January 3, 2014

    LIFEPRO COLD THERAPY MACHINE FOR (ANKLE, CALF, THIGH) WITH REMOTE AND 5 COMPRESS

    FDA Adverse Event
    Injury ·LIFEPRO FITNESS LLC·Product code IRP·November 1, 2022

    INNOVA 2000

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS SCS·Product code MQB·October 13, 2010

    UNKNOWN PARIETEX PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·February 7, 2022

    Mono Mo a Hu CD64, Fc Gamma Receptor I/RPE, Cl 10.1

    FDA UDI
    AGILENT TECHNOLOGIES SINGAPORE PTE LTD·05700572204466·Monoclonal Mouse Anti-Human CD64, Fc Gamma Rec...

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·January 21, 2022

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·October 12, 2018

    TALENT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 18, 2014

    UNKNOWN SHOULDER LOCKING SCREW

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·June 24, 2024

    UNK SHOULDER HUMERAL EPIPHYSIS DELTA XTEND

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code HSD·June 24, 2024

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·November 27, 2024

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 22, 2019

    IMMULITE /IMMULITE 1000 Systems TIE Total IgE, REF LKIE1, SMN 10380867, IVD --- Siemens Healthcare Diagnostics Products Ltd. For in vitro diagnostic use with the IMMULITE, IMMULITE 1000, and IMMULITE 2000/ IMMULITE 2000 XPi Systems Analyzers - for the quantitative measurement of Total Immunoglobulin type E (IgE) in serum.

    FDA Enforcement
    Class II ·Terminated·Siemens Healthcare Diagnostics·May 7, 2014

    ADVIA Centaur Systems Insulin Calibrator; Test Code: Calibrator IRI; Catalog Number: 04618899

    FDA Enforcement
    Class II ·Terminated·Siemens Healthcare Diagnostics, Inc·May 24, 2017

    1.5T LINX, 14B

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·October 28, 2021

    AIR COMPRESSION LEG MASSAGER

    FDA Adverse Event
    Injury ·SHENZHEN DONGJILIAN MEDICAL TECH CO., LTD·Product code IRP·June 14, 2024

    1.5T LINX, 14B

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·June 5, 2019

    LINX 1.5T 14 BEAD OUS

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·February 24, 2023