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

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    STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Arthrex DX Reinforcement Matrix

    FDA UDI
    DSM BIOMEDICAL, INC.·00812337020022·

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540489708·BASIC ORBITAL FLOOR PLATE, MEDIUM

    Arthrex DX Reinforcement Matrix

    FDA UDI
    DSM BIOMEDICAL, INC.·M263ABS30002·

    Acosta Uro-Gard

    FDA UDI
    Acosta Medical Group, Inc.·10860012266811·Uro-Gard Urine Collection Bag

    Tenex Health TX®

    FDA UDI
    TENEX HEALTH, INC.·10857156006076·TX-Bone (TXB) Procedure Pack, Shelf Pack, No Su...

    Insurgical, Inc.

    FDA UDI
    Insurgical, Inc.·00860007230073·14.4v Battery Pack Assembly

    Tenex Health TX®

    FDA UDI
    TENEX HEALTH, INC.·10857156006144·TX2 Procedure Pack, Shelf Pack, No Supply Kit

    Tenex Health TX®

    FDA UDI
    TENEX HEALTH, INC.·10857156006205·TX1 Procedure Pack, Shelf Pack, No Supply Kit

    PancreasPak

    FDA UDI
    Paragonix Technologies Inc·00850005470045·PancreasPak SherpaCool

    Diamondback Peripheral

    FDA UDI
    Cardiovascular Systems, Inc.·10852528005824·Diamondback Peripheral, Exchangeable Series, 1....

    BD SPINAL NEEDLE 27GA 3.50 IN

    FDA Adverse Event
    Malfunction ·Product code BSP·July 21, 2021

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    HARDY DISK, PENICILLIN, 10 UNITS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·October 19, 2006

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·October 19, 2006

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 13, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 28, 2011

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 21, 2008

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·May 6, 2022