BEUDAMED
    607 results · 24ms · 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 ×

    360CAS Knee

    FDA 510(k)
    FDA Class 2 ·Neurology

    NA

    FDA UDI
    Medos International Sàrl·10886705028788·HD EP Arthroscope/Sinuscope compatible with Sto...

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955746064·INTROCAN SAFETY 2 W PUR 20GX32MM - US

    Symmetry Charnley

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482061091·Symmetry® Retractor, Charnley Blade, Short Blad...

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517070675·

    Probe Cover: JZ-KBT-001, JZ-KBT-002, JZ-KBT-005, JZ-KBT-007, JZ-KBT-008, JZ-KBT-009, JZ-KBT-010, JZ-KBT-015, JZ-KBT-025, JZ-KBT-026

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MARK III PHASED ARRAY SHOULDER COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·October 14, 2009

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 24, 2009

    ORTHOPAT PERIOPERATIVE AUTOTRANSFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORP.·Product code CAC·October 24, 2011

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 15, 2012

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·September 9, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·August 24, 2009

    VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 24, 2009

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·August 24, 2009

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 24, 2009

    POLYSORB SUTURE

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GAM·March 5, 2009

    XCEL DILATING TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·February 24, 2009