BEUDAMED
    21 results · 65ms · 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.

    LMA NORTH AMERICA INC

    FDA Adverse Event
    Malfunction ·*·Product code CAE·January 30, 2006

    LARYNGEAL MASK AIRWAY

    FDA Adverse Event
    Malfunction ·THE LARYNGEAL MASK COMPANY·Product code CAE·August 17, 2001

    LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device is to be used as an adjunct to assess intubation. Its purpose is not to eliminate clinical judgment

    FDA Recall
    Terminated ·LMA North America Inc·Product code BTR·May 23, 2012

    FASTRACH

    FDA Adverse Event
    LMA NORTH AMERICA, INC·Product code BTR·February 2, 2010

    LMA NORTH AMERICA

    FDA Adverse Event
    Death ·LMA NORTH AMERICA, INC.·Product code CAE·September 26, 2003

    LMA

    FDA Adverse Event
    Injury ·LMA NORTH AMERICA, INC.·Product code CAE·June 28, 2007

    LMA NORTH AMERICA LMA - CLASSIC

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code CAE·May 5, 1999

    PAINCARE 3000

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code MEB·November 29, 2010

    FASTRACH ETT

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code BTR·January 16, 2007

    *

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code CAE·December 21, 2006

    LMA

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code CAE·November 28, 2007

    LMA FASTRACH ETT (SINGLE USE) 7.0MM/9.8MM OD

    FDA Adverse Event
    Malfunction ·LMA NORTH AMERICA, INC.·Product code CAE·July 9, 2007

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA CLASSIC

    FDA Adverse Event
    Other ·LMA NORTH AMERICA, INC.·Product code CAE·April 29, 2002

    LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size 4, Catalog No. 12150, Lot FJ021202

    FDA Recall
    Terminated ·LMA North America Inc·Product code CAE·June 18, 2003