BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    PROTECTRODE SYSTEMS CONCENTRIC

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Nu-Edge Cobalt Chromium Brackets

    FDA UDI
    TP ORTHODONTICS INC·00192029046845·LR 1st BI W/DISTALHK Torque -12, Tip +2 0.46mm ...

    Ophthalmic Hook

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103296·LESTER IOL MANIPULATOR VAULTED ANGLED

    ZOLL AUTOCLAVABLE INTERNAL HANDLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABL90 FLEX

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 29, 2013

    AVAULTA BIOSYNTHETIC SUPPORT SYSTEM- ANTERIOR

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·November 19, 2010

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIM·July 14, 2014

    CEMENTED FINNED TIB. TRA SZ 3F/3T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 28, 2025

    OPTETRAK THREE PEG PATELLA 38MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 6, 2024

    THREE PEG PATELLA 41MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 3, 2024

    CEMENTED FINNED TIB. TRA SZ 2F/2T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 23, 2024

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 1, 2024

    Bard Aspira Valve Assembly/Repair Kit, Product Code 4991506. The Aspira Peritoneal Drainage system is indicated for intermittent drainage of recurrent and symptomatic malignant ascites. The catheter is intended for long-term access of the peritoneal cavity in order to relieve symptoms such as dyspnea or other symptoms associated with malignant ascites.

    FDA Recall
    Terminated ·Bard Access Systems·Product code FJS·May 21, 2011

    Bard Aspira Luer Adapter, Product Code 4991505. The Aspira Peritoneal Drainage system is indicated for intermittent drainage of recurrent and symptomatic malignant ascites. The catheter is intended for long-term access of the peritoneal cavity in order to relieve symptoms such as dyspnea or other symptoms associated with malignant ascites.

    FDA Recall
    Terminated ·Bard Access Systems·Product code FJS·May 21, 2011

    Bard Aspira Dressing Kit, Product Code 4991503. The Aspira Peritoneal Drainage system is indicated for intermittent drainage of recurrent and symptomatic malignant ascites. The catheter is intended for long-term access of the peritoneal cavity in order to relieve symptoms such as dyspnea or other symptoms associated with malignant ascites.

    FDA Recall
    Terminated ·Bard Access Systems·Product code FJS·May 21, 2011