BEUDAMED
    113 results · 31ms · Sources: EU EUDAMED, US FDA

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    Vial2Bag Advanced 20mm Admixture Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257010112·M.3 SOFT OA BRACE, VARUS, RIGHT, XL

    UP - Vehicle - 380-55230 - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014173·UP - Vehicle - 380-55230 - 18 Metal

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707183943·Accufit Molar Bands Lower Right First Molar 41 1/2

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019644·1.5mm Drill, J-Latch

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383556361·"An absorbent paper points is an endodontic pap...

    LIQUICHEK URINE TOXICOLOGY CONTROL LEVEL C2 LOW OPIATE & C3 LOW OPIATE MODELS 468 & 469

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    THERACLEAR

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

    CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830

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

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·October 14, 2014

    STRYKER TRIATHLON TIBIAL BEARING INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS·Product code JWH·October 27, 2015

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·April 8, 2014

    MINIBORE PCA EXTENSION SET -67 I

    FDA Adverse Event
    Injury ·HOSPIRA·Product code LJS·November 21, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 27, 2015

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 23, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 30, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 13, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 26, 2014

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 16, 2014

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·July 6, 2018