BEUDAMED
    10,000 results · 45ms · 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 ×

    0413,APS1,08,N,RA

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152372·0413,APS1,08,N,RA

    0800,APS0,08,AV,N,RA

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828149280·0800,APS0,08,AV,N,RA

    0412,APS1,08,N,RA(6&8)

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152280·0412,APS1,08,N,RA(6&8)

    0800,APS0,08,N,RA,RDL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828155755·0800,APS0,08,N,RA,RDL

    0800,APS1,08,N,RA,VL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828149235·0800,APS1,08,N,RA,VL

    0307,APS1,08,N,RA,CW

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828149648·0307,APS1,08,N,RA,CW

    0413,APS1,08,N,RA,SF

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152488·0413,APS1,08,N,RA,SF

    1500,APS1,08,N,RA,TY,RDL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828150200·1500,APS1,08,N,RA,TY,RDL

    0800,APS1,08,N,RA,SJ,RDL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828153041·0800,APS1,08,N,RA,SJ,RDL

    1602,APS1,08,N,RA,CH,RGL,STD

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828150446·1602,APS1,08,N,RA,CH,RGL,STD

    INCEPTIV

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 29, 2025

    QUILL

    FDA Adverse Event
    Injury ·SURGICAL SPECIALTIES CORPORATION·Product code NEW·January 29, 2024

    OXF ANAT BRG RT MD SIZE 7 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·November 22, 2021

    UNKNOWN KNEE CONSTRUCT LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 25, 2024

    UNKNOWN KNEE CONSTRUCT ATTUNE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 25, 2024

    STAR S4 IR

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code LZS·April 22, 2025

    Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable anaesthesia sets. Product Usage: The breathing bag is a component of the anesthesia set (breathing circuit) that is intended to is the conduit for administering medical gases to a patient during ventilation. It provides both an inspiratory and expiratory route. 2. The test lung is an apparatus that contains a breathing bag and and connector. It is connected to the output of a ventilator and is used as part of the device/system check out.

    FDA Enforcement
    Class II ·Terminated·Draeger Medical, Inc.·April 16, 2014

    Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable anaesthesia sets. Product Usage: The breathing bag is a component of the anesthesia set (breathing circuit) that is intended to is the conduit for administering medical gases to a patient during ventilation. It provides both an inspiratory and expiratory route. 2. The test lung is an apparatus that contains a breathing bag and and connector. It is connected to the output of a ventilator and is used as part of the device/system check out.

    FDA Recall
    Terminated ·Draeger Medical, Inc.·Product code BZO·March 25, 2014

    Naera Hospital Bassinet, Model No. 4402

    FDA Recall
    Terminated ·Stryker Medical Division of Stryker Corporation·Product code NZG·October 10, 2018

    OXFORD UNICOMPARTMENTAL KNEE CEMENTLESS RIGHT MEDIAL TIBIAL TRAY SIZE AA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·October 21, 2016