BEUDAMED
    10,000 results · 206ms · 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 ×

    LRM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AM-25 L RM

    FDA UDI
    W & H Dentalwerk Bürmoos GmbH·J021301020001·Air Motor

    TG-97 L RM Synea Fusion

    FDA UDI
    W & H Dentalwerk Bürmoos GmbH·J021301970001·

    TG-98 L RM Synea Fusion

    FDA UDI
    W & H Dentalwerk Bürmoos GmbH·J021301980001·Synea Fusion Highspeed Handpiece

    AM-25 L RM Air Motor

    FDA UDI
    W & H Dentalwerk Bürmoos GmbH·J021301020011·Air Motor

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902194302·Pressure Injectable Arrowg+ard Blue Advance(R) ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902189353·Pressure Injectable Arrowg+ard Blue Advance(R) ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902169911·Pressure Injectable Arrowg+ard Blue Advance(R) ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902169928·Arrowg+ard Blue Advance(TM) PICC Kit pre-loaded...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902194296·Pressure Injectable Arrowg+ard Blue Advance(R) ...

    Stern Weber

    FDA UDI
    CEFLA SOCIETA' COOPERATIVA·08033837933670·The device is a dental unit consisting of compo...

    ZOLL-DENTAL

    FDA UDI
    Zoll-Dental·00840105210375·Prichard PR-3 L/R-M

    Stern Weber

    FDA UDI
    CEFLA SOCIETA' COOPERATIVA·08033837933687·The device is a dental unit consisting of compo...

    Stern Weber

    FDA UDI
    CEFLA SOCIETA' COOPERATIVA·08033837933694·The device is a dental unit consisting of compo...

    CSI,30G 300-014

    FDA Adverse Event
    Malfunction ·BRIVANT LTD. T/A LAKE REGION MEDICAL·Product code DQX·March 7, 2019

    LRM PRODUCES GUIDEWIRES ON AN OEM BASIS FOR MANUFACTURERS,KIT ASSEMBLERS, AND DISTRIBUTORS.

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 18, 2025

    illumina Model NextSeq 550 Dx REF 20005715

    FDA Recall
    Completed ·Illumina, Inc.·Product code PFF·May 3, 2022

    illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx

    FDA Recall
    Completed ·Illumina, Inc.·Product code PFF·May 3, 2022

    NITREX NITINOL GUIDEWIRE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code DQX·March 24, 2017