BEUDAMED
    11 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 ×

    Relieva Tract Balloon Dilation System

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    OSE

    FDA UDI
    ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042123359·1000 Stainless Steel Ligature Ties - .009

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515068414·Gelpi Ret, shrp tips, 3 1/2"

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515027596·Gelpi Ret, shrp tips, 3 1/2"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197032285·Jacobson Micro Scissors 165mm/...

    LEVEEN SUPERSLIM NEEDLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SPECTRA OPTIA R APHERESIS SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNIV RNGLC SHL 52MM/L23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 13, 2024

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

    HEARTWARE HVAD

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011