BEUDAMED
    33 results · 37ms · 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.

    ORTHO ALL-FLEX DIAPHRAGM

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

    Molift

    FDA UDI
    Etac A/S·05707995036063·

    Berman Airways

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043800409·

    8.0 X 80mm Cann Screw Fastener 40mm Var Thd

    FDA UDI
    Osteocentric Technologies, Inc.·00810074306782·8.0 X 80mm Cann Screw Fastener 40mm Var Thd

    Ø7.0 x 40mm x 80mm CANNULATED PARTIAL THREAD SCREW

    FDA UDI
    Osteocentric Technologies, Inc.·00816950026980·Ø7.0 x 40mm x 80mm CANNULATED PARTIAL THREAD SCREW

    Vermed

    FDA UDI
    GRAPHIC CONTROLS ACQUISITION CORP·00009336001170·Electrocardiographic recording paper

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933783·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933172·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955934391·Percutaneous Transluminal Angioplasty Balloon C...

    VADER Pedicle System, Rod, Ti, Straight, Ø 6.0 r000 x 400 mm

    FDA UDI
    icotec AG·07640164847252·VADER Pedicle System, Rod, Ti, Straight, Ø 6.0 ...

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 16, 2024

    INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED

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

    SLEEVED FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 5, 2024

    TREK¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code LOX·January 7, 2026

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 26, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 6, 2011

    POLYFLUX LR CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code MSF·July 24, 2008

    2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·November 30, 2016

    GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·December 28, 2016