BEUDAMED
    53 results · 23ms · Sources: EU EUDAMED, US FDA

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    URINE CANNABINOIDS (THC) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 95A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092117200·NobelBiocare™ Tri-Lobe-compatible NP X 4.5mm En...

    Preat

    FDA UDI
    Preat Corporation·00842092170571·NobelBiocare™ Tri-Lobe-compatible NP X 4.5 mm E...

    TEWA

    FDA UDI
    asia-med GmbH·04251282510305·TeWa CJ-Type 2013 (s): uncoated acupuncture ne...

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282502980·TeWa CJ-Type 2013 (s): uncoated acupuncture ne...

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700004610·

    MASEL Buccal Tubes

    FDA UDI
    Ortho Organizers, Inc.·00190707102296·BT 022 ROTH MINI SGL U7L DB (10)

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700004610·

    MINXRAY HF70D HIGH FREQUENCY PORTABLE DENTAL X-RAY UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    HARDYDISK, PIPERACILLIN/TAZOBACTAM, 110MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FUTURE DIAGNOSTICS B.V. STAT-INTRAOPERATIVE INTACT PTH KIT

    FDA Adverse Event
    FUTURE DIAGNOSTICS B.V.·Product code CEW·November 1, 2017

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 4, 2022

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 12, 2013

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTR·February 14, 2011

    PULMONETIC

    FDA Adverse Event
    Injury ·CARDINAL HEALTH 203/PULMONETIC SYSTEM, INC.·Product code CBK·February 21, 2008

    INSTINCT JAVA

    FDA Adverse Event
    Injury ·ZIMMER SPINE·Product code NKB·May 13, 2016

    POLARIS 5.5 INSTRUMENTS

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code HXX·May 22, 2015

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code FCW·March 26, 2019

    SHORT MAS INSERTER

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code HXX·May 22, 2015

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·November 18, 2024