BEUDAMED
    7 results · 19ms · 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 ×

    MODIFICATION TO MEDI-JECT CORPORATION MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    102 P37,NURSE ONLY,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101011·102 P37,NURSE ONLY,STKR

    Transvaginal Access Platform

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LATERAL COLUMN LENGTH PLATE, MODEL 824073000-3, LOCKED FUSION PLATE, MODEL 824077010, COMPRESSION FUSION PLATE,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PENUMBRA SYSTEM REPERFUSION CATHETER 5MAX

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 6, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    VIRTUOSO II VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014