BEUDAMED
    7 results · 13ms · Sources: EU EUDAMED, US FDA

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    Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

    FDA Recall
    Terminated ·Candela Corporation·Product code GEX·September 10, 2019

    Canister HFC-134a / 980g, ALUM Product Number: 1600-00-0223 Revision .0C Coolant canister for use with surgical laser.

    FDA Recall
    Terminated ·Candela Corporation·Product code GEX·September 10, 2019

    Canister HFC-134a /980g, ALUM, 15 pack Product Number: 1600-00-0224 Revision .0C Coolant canister for use with surgical laser.

    FDA Recall
    Terminated ·Candela Corporation·Product code GEX·September 10, 2019

    Canister HFC-134a /1000g, ALUM, 15 pack Product Number: 1600-00-0219 Revision .0C Coolant canister for use with surgical laser.

    FDA Recall
    Terminated ·Candela Corporation·Product code GEX·September 10, 2019

    Gelzone Shoulder Sleeve, Catalog Number SLV634, Lot Number 852766. Product Usage: To be used where limb support and/or elevation is considered necessary.

    FDA Recall
    Terminated ·Implantech Associates Inc·Product code HST·January 29, 2014

    Trilogy 100, 200 and 202 Ventilators The device is intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation.

    FDA Recall
    Terminated ·Respironics, Inc.·Product code CBK·October 11, 2011

    SEDASYS Computer-Assisted Personalized Sedation System, SEDPRU01. An integrated physiological monitoring and drug delivery system intended to provide physician-led teams with a means of administering 1% propofol (10 mg/mL) injectable emulsion to sedate patients > 18 (ASA I-II) undergoing esophagogastroduodenoscopy (EGD) and colonoscopy procedures. Intended to provide physician-led teams with a means of administering 1% propofol (10 mg/mL) injectable emulsion to sedate patients > 18 (ASA I-II) undergoing esophagogastroduodenoscopy (EGD) and colonoscopy procedures.

    FDA Recall
    Terminated ·Ethicon Endo-Surgery Inc·Product code PDR·May 13, 2015