BEUDAMED
    33 results · 41ms · Sources: EU EUDAMED, US FDA

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    G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular System Vivacit-E Vitamin E Highly Crosslinked Polyethylene

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

    RINGLOC-X E1 H/W 56/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 27, 2026

    BIOLOX DELTA CER LNR 40MM G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 27, 2026

    AVAN E1 INSERT 28 S 52

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 6, 2025

    BIOLOX DELTA CER LNR 32MM E

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 8, 2025

    RINGLOC BIPOLAR VIVACIT-E

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·November 13, 2025

    BIOLOX DELTA LNR 40MM 58-60MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·August 21, 2025

    BIOLOX DELTA LNR 36MM 62-70MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 20, 2024

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 22, 2025

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·March 28, 2025

    BIOLOX DELTA CER LNR 36MM F

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 14, 2025

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·March 28, 2025

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543290·ROD BENDER MODULAR TIP, 6.0mm

    AIRWAY BALLOON CATHETER INFLATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    INFRARED EAR THERMOMETER MODEL DR. SCHVEN ICT-1000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 6, 2008

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 26, 2013

    MX-PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·July 29, 2011