BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLEARLINK BURETROL SOLUTION SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 13, 2023

    G7 ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYSTEM 100 ULTRAFILTRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    G7 SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·April 24, 2026

    MODULAR CUP SYSTEM, RIMCUP

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 21, 2026

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    GII

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·May 22, 2013

    ASKU

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·June 14, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 15, 2008

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    G7 BONEMASTER LTD ACET SHL 58G

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019

    G7 FINNED BM 3 HOLE SHELL 48C

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018

    DURAL ALPHA INSERT NEUTR JJ/36

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·February 18, 2026

    G7 BONEMASTER LTD ACET SHL 46B

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·July 18, 2019

    G7 BONEMASTER LTD ACET SHL 52E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 14, 2018