BEUDAMED
    279 results · 48ms · 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.

    ALTUS COOLGLIDE

    FDA Adverse Event
    ALTUS MEDICAL, INC.·Product code GEX·May 8, 2003

    INPEN MMT-105NNBLNA NOVO NORDISK BLUE

    FDA Adverse Event
    Malfunction ·COMPANION MEDICAL INC·Product code FMF·June 1, 2021

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 13, 2023

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 13, 2023

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·November 1, 2023

    Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03

    FDA Recall
    Terminated ·TZ Medical Inc.·Product code FRO·October 14, 2015

    Aeroneb Go Micropump Nebulizer Featuring OnQ electronic micropump, RX, Manufactured by Medical Industries America Inc., Adel, IA. The product is sold individually or in master packs of 8 under the following model numbers (all using the same box label): Model 7000 - Consisting of the Aeroneb Go, battery controller, battery controller cable, 3 AA alkaline batteries, mask elbow, mouthpiece, carry bag, and user manual; Model 7030 - Consisting of the Aeroneb Go, AC wall adapter, mask elbow, mouthpiece, carry bag, and user manual; Model 7070 - Consisting of the Aeroneb Go, battery controller, battery controller cable, 3 AA alkaline batteries, AC wall adapter, mask elbow, mouthpiece, carry bag, and user manual; Model 7000-1 - Consisting of the Aeroneb Go, battery controller, battery controller cable, 3 AA alkaline batteries, European mask elbow, mouthpiece, carry bag, and user manual; Model 7030-1 - Consisting of the Aeroneb Go, AC wall adapter, European mask elbow, mouthpiece, carry bag, and user manual; Model 7070-1 - Consisting of the Aeroneb Go, battery controller, battery controller cable, 3 AA alkaline batteries, AC wall adapter, European mask elbow, mouthpiece, carry bag, and user manual. 7000LINCARE - Consisting of the Aeroneb Go, battery controller with a Lincare private label cover plate, battery controller cable, 3 AA alkaline batteries, mask elbow, mouthpiece, carry bag, and user manual; 7070LINCARE - Consisting of the Aeroneb Go, battery controller with the Lincare private label cover plate, battery controller cable, 3 AA alkaline batteries, AC wall adapter, mask elbow, mouthpiece, carry bag, and user manual.

    FDA Recall
    Terminated ·Medical Industries America Inc·Product code CAF·September 7, 2004

    See Luer Cap Set, MPC-130, set, administration, intravascular

    FDA Recall
    Open, Classified ·Molded Products Inc·Product code FPA·February 17, 2026

    XiO Radiation Treatment Planning System, XiO Release 4.3.0 through 4.50.00. Used to create treatment plans for any cancer patient for who external beam radiation therapy or brachytherapy has been prescribed.

    FDA Recall
    Terminated ·Computerized Medical Systems Inc·Product code muj·May 13, 2009

    Hydrophobic HALO360 Filter that is packaged with HALO360+ Ablation Catheters Model numbers 32041-22, 32041-28, 32041-31 and 32041-34, and/or with HALO360 Sizing Balloon Model number 3441B.

    FDA Recall
    Terminated ·Barrx Medical, Inc.·Product code GEI·September 18, 2008

    Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number: 332252. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879, 551994, 552024. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993, 552051, 552083, 552119, 555569. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075, 332266. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017