BEUDAMED
    33 results · 24ms · 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 ×

    Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517578280·CoRoent Ant TLIF Ti 10x10x32mm 8°

    INSIGHT

    FDA UDI
    CARESTREAM HEALTH, INC.·40889971200323·INSIGHT 75PKT 22x35 film IP01C

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896054745·METZENBAUM SCISSORS CURVED BLADES POWER CUT GOLD

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180149861·CLEANING BRUSH FOR 10 MM TROCAR SLEEVE, EACH

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828160186·GEN4 DIGITAL

    Adapter for Hoses

    FDA UDI
    NORTHGATE TECHNOLOGIES INC.·00817183020646·

    MICROSCAN SYNERGIES PLUS GRAM NEGATIVE MIC/COMBO PANELS WITH CEFUROXIME (1-64 UG/ML)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTRATHECAL CATHETER

    FDA Adverse Event
    Injury ·NEUROLOGICAL DIVISION, MEDTRONIC INC·Product code LKK·July 24, 2007

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 10, 2021

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code LZG·October 26, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    ANCURE ENDOGRAFT

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·July 17, 2008

    MODULAR FEM STEM PRESS-FIT PLASMA SPRAYED CEMENTLESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·October 21, 2020

    IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 17, 2017

    IMMERSION HYDROBATH

    FDA Adverse Event
    Malfunction ·INVACARE CLEVELAND STREET·Product code ILJ·October 24, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·July 1, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·April 8, 2021