BEUDAMED
    19 results · 27ms · 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 ×

    PG Pro Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365104121·

    WAVESTATE NEUROMONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    VEGA CPAP SYSTEM/HEATED HUMIDIFIER, MODEL CP-03

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FEMORAL POSTERIOR AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    LASER HAIR GROWTH CAP

    FDA Adverse Event
    Injury ·UNKNOWN·Product code OAP·February 26, 2025

    STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIA FIXED CEMENTED LEFT SIZE D STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·October 22, 2014

    1.5MM RAPID RESORBABLE CORTEX SCREW 4MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JEY·June 27, 2013

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2011