BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Leadtek Fingertip Pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Contrast Line

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333207343·Contrast Line 10"(25cm) Male/Female PVC 1200 PSI

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E8961933500·Laster Retractor, for upper impacted wisdom...

    BRIVO NM 615

    FDA 510(k)
    FDA Class 2 ·Radiology

    ECLIPSE SOFT TISSUE FASTENER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 23, 2025

    MATNEU SCR Ø1.5 SELF-DRILL L4 TAN 4U I/C

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 27, 2013

    HYDRATOME RX SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 7, 2008

    ZIMMER NATURAL NAIL

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·July 28, 2011

    dS Breast 7ch 1.5T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 4, 2024