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

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    Emprint Ablation System with Thermosphere Technology

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

    POWER SUPPLY: ASSEMBLY FOR ROSI

    FDA UDI
    VASCULAR TECHNOLOGY, INCORPORATED·00817122020423·Part Number 200796, POWER SUPPLY: ASSEMBLY FOR ...

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825003760·Steerable Diagnostic EP Catheter , LARGE 4.0, 8...

    BRUNNER RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896019737·BRUNNER RETRACTOR

    MAGIC MOBILITY 4 X 4 WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CARD IQ ANALYSIS II

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·May 12, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 15, 2025

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·January 7, 2019

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 29, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 17, 2026

    QUICK SET PARADIGM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·November 2, 2009

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 24, 2014

    EXTRACTOR ASNIS III FOR SCREWS:Ø4.0MM AO FITTING

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-SELZACH·Product code LXH·July 2, 2013

    Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·January 30, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 1, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·November 21, 2024

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·February 26, 2026