BEUDAMED
    11 results · 25ms · 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 ×

    Q-FLO CLOSED MALE LUER CONNECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SafeGuide® Single

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734023310·Disposable Over the Guidewire Esophageal Dilato...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450851432·

    ARM-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WRIST-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRANSRADIAL ARTERY ACCESS DEVICES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANTHEM RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    2.7MM LCP(TM) CONDYLAR PLATE 7 HOLES SHAFT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·May 21, 2013

    ALTRX +4 10D 36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 2, 2011

    Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.

    FDA Enforcement
    Class II ·Ongoing·Philips North America·May 6, 2026

    Artis Q biplane, Model Number 10848282

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·April 27, 2022

    Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·September 7, 2022