BEUDAMED
    10 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 ×

    SeaSpine Beachside System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Edge™ Diamond FR023-5.5F Football Round

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172003018·Diamond dental bur, reusable

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583032825·ET20, KIT 312 2.4G NFM 85 R BE ENCHANT 20

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 12, 2022

    XIO RTP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·October 7, 2008

    PLV-102

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·June 20, 2013

    LIGACLIP ENDOSCOPIC ROTATING MCA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 6, 2017