BEUDAMED
    36 results · 27ms · Sources: EU EUDAMED, US FDA

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    EASYQC - CHEMISTRY WITH ELECTROLYTES; CHEMISTRY; ELECTROLYTES KIT; CHEMISTRY CALIBRATOR, CREA-U CLAIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004042·PowerChem Neoprene Exam Gloves, Large

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014606118·AXILLARY ROLL 8"LX4"DIA 3/4" MEMORY FOAM WRAPP...

    iDuo® Patella Trial

    FDA UDI
    Conformis, Inc.·00850268007385·iDuo® 38mm Patella Trial Reusable Instrument

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450181164·

    Azur Pure Helical

    FDA UDI
    Microvention, Inc.·00810170018138·Azur

    EXEL I.V. ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PC ECG 1200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADULT INSPIRATORY HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·November 17, 2009

    EQUINOXE PRIMARY SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 28, 2022

    PELVISOFT ACELLULAR COLLAGEN BIOMESH

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABORATORIES·Product code FTM·April 24, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 6, 2011

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON EDNO-SURGERY, LLC·Product code LFL·July 24, 2008

    AVISTA? MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 23, 2026

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 29, 2026

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 9, 2026

    ECHELON 60

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 29, 2026

    ADULT DUAL HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·September 14, 2011

    Guidant Rapido 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Lenght 54 cm, Coronary Sinus - Extended Hook Right Tip Shape, CS-EH R, REF 7592

    FDA Recall
    Terminated ·Guidant Corp-Cpi Division·Product code DQR·March 11, 2004

    DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 28 cm Straight Basic Kit, Catalog Number/REF 10302804, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

    FDA Recall
    Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010