BEUDAMED
    9 results · 31ms · 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 ×

    VRESELECT CULTURE MEDIUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ZrLiquid HT A3-S 100ml

    FDA UDI
    ARGEN CORPORATION, THE·D818122187·Dental porcelain/ceramic restoration kit

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 19, 2023

    PRESSURE WIRE SENSOR, MODELS 12003/12303, 12004/12304

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RII INFRARED EAR THERMOMETER,

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LAP-BAND AP ADJUSTMENT GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 17, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2011

    VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT/OXIMETRY SENSOR

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCE, DR·Product code DRS·August 15, 2008

    SOMATOM Edge Plus-Computed tomography system Model 1026700

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·January 19, 2022