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

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    TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES

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

    REMEL

    FDA UDI
    REMEL, INC.·00848838005893·BHI Agar (slant) 20/PK

    Mini-Mono® Brackets

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70602321·Mini-Mono-Brackets Andrews 'N' .018" 400 Brackets

    Logical Lateralised 20° Hooded Liner

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215095314·

    ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRE-POWDERED NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DESARA BLUE TV

    FDA Adverse Event
    Injury ·CALDERA MEDICAL INC.·Product code OTN·December 5, 2019

    EON PATIENT PROGRAMMER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 11, 2013

    INJECTION GOLD PROBE BIPOLAR CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·June 12, 2008

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·April 15, 2011

    ARCHITECT IPTH REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code CEW·March 19, 2025

    Tubing Set for TEM-Combined System; the tube set consists of a rectal pressure measuring tube, an insufflation tube, an irrigation tube, a suction tube, a pump tube, and a connection tube; a sterile, disposable, single use accessory to the TEM (Transanal Endoscopic Microsurgery) System used for insufflation of the rectal cavity; Manufacturer: Richard Wolf GmbH, Postfoch 1164, D-75343 Knittlingen, Deutschland; Product Number 4170.801

    FDA Recall
    Terminated ·Richard Wolf Medical Instruments Corp.·Product code HIF·July 7, 2006