BEUDAMED
    160 results · 27ms · 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.
    Filters Regulation: Us FDA ×

    Defendo Pentax Single Use Biopsy Valve, Defendo Pentax Single Use Air/Water Valve, Defendo Pentax Single Use Suction Valve, Endogator Pentax Single Use Connector

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694017947·MFx 2.0mm x 4mm Angulated Locking Auto-Drive Screw

    Channel

    FDA UDI
    MEDTRONIC PS MEDICAL, INC.·00643169103597·NEUROENDOSCP 2232-004 CHANNEL 3.5 L 13

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955341856·Introcan Safety 2 - 22G x 1.0 in., PUR, Straight

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369382·THOMAS LEG SPLINT, RADIOLUCENT LARGE

    FEMORAL BODY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 5, 2018

    COCR HEAD, M, 36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LPH·March 28, 2023

    AQUABOSS ECORO DIA 50

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

    NPWT WOUND DRESSING KIT- MEDIUM, NPWT WOUND DRESSING KIT- LARGE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BIOLOX DELTA, CERAMIC FEMORAL HEAD, M,36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·July 3, 2019

    Cable-Ready®

    FDA UDI
    Zimmer, Inc.·00889024039513·

    UNKNOWN ZMR BOWED STEM PROVISIONAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 6, 2018

    FREEDOM ALL POLY CUP 54MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·December 2, 2024

    BREAST IMPLANTS

    FDA Adverse Event
    Malfunction ·MCGHAN MEDICAL CORP·Product code FWM·October 12, 2005

    BI-METRIC/X POR NC LAT 13X145

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 16, 2023

    WAGNER SL REVISION STEM 15/225

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·May 29, 2025

    BLAZER II XP

    FDA Adverse Event
    Injury ·EP TECHNOLOGIES, INC.·Product code LPB·May 3, 2004

    ORCHESTRA

    FDA Adverse Event
    Malfunction ·ELA MEDICAL, S.A.·Product code KRG·May 5, 2004

    REVITAN DIST. CURVED 20/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 10, 2026

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·July 17, 2023