BEUDAMED
    24 results · 38ms · Sources: EU EUDAMED, US FDA

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    HK LIPOSUCTION ASPIRATOR, MODEL AP-III & AP230-III

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Trilogy

    FDA UDI
    Respironics, Inc.·00606959022690·Trilogy 200 Ventilator, Germany

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091032802·Baltic Denture System BDLoad Sw7 PLSEbm6DFs A3,...

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR30328021·Triangular clasps 0,80 mm

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746161599·DB BKT LP LL 2ND BIC 022 T-17 A+2 R=0 OFFSET RA...

    MP3CF ELECTRIC WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    RAPID EXCHANGE TAPERTOME

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    General Instrument

    FDA UDI
    ALPHATEC SPINE, INC.·00840180506042·Curette, Cup, Pull, Straight, Serrated, Size 3

    AMINGO

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 9, 2016

    AMINGO

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 30, 2016

    AMINGO

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 29, 2016

    AMINGO

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 4, 2017

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 23, 2020

    TRANSPAC® IV MONITORING KIT W/03 ML SQUEEZE FLUSH DEVICE, SAFESET¿ RESERVOIR, 84

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·March 23, 2023

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 3, 2013

    ARMADA 14 PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·March 29, 2011

    DEEP BRAIN STIMULATION LEAD KIT

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·April 23, 2008

    TRANSPAC® IV MONITORING KIT W/03 ML SQUEEZE FLUSH DEVICE, SAFESET¿ RESERVOIR, 84

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·October 27, 2023

    VERSYS FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 16, 2016

    Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.

    FDA Enforcement
    Class I ·Ongoing·Philips Respironics, Inc.·July 21, 2021