BEUDAMED
    13 results · 20ms · 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 ×

    TRACHEOSTOMY CARE KIT (STERILE)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094192505·Nipple Sizers

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110942·STERILIZING CASE PLASTIC SMALL

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937903·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939075·Percutaneous Transluminal Angioplasty Balloon C...

    Sapphire ULTRA Coronary Dilatation Catheter

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955979262·

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955936739·Percutaneous Transluminal Angioplasty Balloon C...

    ERYTYPE S ABD REV. A1&B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·November 25, 2010

    SLIDEX STREPTO-KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CARDIO-CARD ECG MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GENDER SOLUTIONS NK FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 17, 2013

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·November 22, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014