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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    EMS AIRFLOW Prophylaxis Master, EMS AIRFLOW One

    FDA 510(k)
    FDA Class 2 ·Dental

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583033365·ENCHANT 40 B 105 FW 3.0

    ProEtch

    FDA UDI
    SILMET LTD·07290016787467·Dental Adhesive

    CETRA

    FDA UDI
    Orthofix US LLC·18257200120314·1-LEVEL PLATE ASSEMBLY, 24MM

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101094·HELVESTON "BIG BARBIE" RETRACTOR 9MM

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306821998·Shapleigh Ear Loop - #3, 13cm

    GRYPHON P BR DS ANCHOR W/ORTHOCORD,GRYPHON P BR ANCHOR W/ORTHOCORD, MODEL 210813,210814

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FASTX STERNAL INTRAOSSEOUS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CUSTOM ACETABULAR-PELVIS LEFT

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LPH·December 17, 2019

    ENDOPATH THORACIC ENDO LINEAR CUTTER RELOAD

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY INC·Product code GAG·December 15, 1997

    EARLYVUE VS30 VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code DSJ·September 15, 2021

    EARLYVUE VS30 VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code DSJ·March 1, 2022

    ENDOPATH THORACIC ENDO LINEAR CUTTER RELOAD

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY INC·Product code GAG·December 15, 1997

    ENDOPATH THORACIC ENDO LINEAR CUTTER RELOAD

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY INC·Product code GAG·December 15, 1997

    CETRA

    FDA Adverse Event
    Malfunction ·ORTHOFIX MEDICAL INC·Product code KWQ·September 18, 2023

    EARLYVUE VS30 VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code DSJ·August 1, 2022

    INOUE BALLOON CATHETER

    FDA Adverse Event
    Injury ·TORAY INDUSTRIES, INC.·Product code MAD·June 27, 2019

    9900

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

    TRUETRACK

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·September 18, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·June 30, 2011