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

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    ASPIRE HD PLUS, ASPIRE HD-S

    FDA 510(k)
    FDA Class 2 ·Radiology

    LARGE CANNULATED SCREWS

    FDA UDI
    Smith & Nephew, Inc.·03596010064202·CANNULATED HIP PIN 130MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694055581·1.2mm Orbital Floor Plate, Pick, .5mm Thick

    ACUSON

    FDA 510(k)
    FDA Class 2 ·Radiology

    WVSM (WIRELESS VITAL SIGNS MONITOR), MODEL 5.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 21, 2013

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEATHCARE CORPORATION·Product code KDI·September 26, 2014

    UNKNOWN DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 2, 2011

    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