BEUDAMED
    26 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 ×

    KINGSCROSS PL-C+B-10, KINGSCROSS PL-C+B-12, KINGSCROSS PL-C+B-08, KINGSCROSS B

    FDA 510(k)
    FDA Class 2 ·Dental

    ArgenZ HT+ 98x18 A4

    FDA UDI
    ARGEN CORPORATION, THE·D818122039·Dental porcelain/ceramic restoration kit

    ELEVANCE

    FDA 510(k)
    FDA Class 1 ·Dental

    COPAN MSWAB COLLECTION, TRANSPORT AND PRESERVATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·December 26, 2012

    EZ STEER THERMOCOOL NAVIGATIONAL BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·June 13, 2011

    NAVI-STAR¿ THERMO-COOL¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·September 12, 2012

    UNSPECIFIED SYSTEM

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·May 16, 2013

    ZIMMER BLOOD REINFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code CAC·May 24, 2011

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code FZP·August 14, 2008

    EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·July 26, 2012

    NAVISTAR® THERMOCOOL®

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·January 30, 2017

    CELSIUS? THERMO-COOL? ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·June 10, 2013

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·September 19, 2012

    GLENOSPHERE DIA. 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MBF·March 15, 2024

    EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·December 5, 2012

    THERMOCOOL SMARTTOUCH SF

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·September 21, 2017

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·June 10, 2013

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·June 10, 2013

    STOCKERT 70 RF GENERATOR

    FDA Adverse Event
    Injury ·STOCKERT GMBH·Product code DRF·July 15, 2013