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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    RAYNER SINGLE USE SMALL INCISION DISPOSABLE INJECTOR, MODEL R-INJ-06

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16740814550·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674081455060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X0814550·8mm H x 14mm W x 55mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X081455120·8mm H x 14mm W x 55mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X08145580·8mm H x 14mm W x 55mm L x 8 degrees XLIF

    ACCUWELL TSH, MODEL KAW-TSH-960

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BIOMET ONCOLOGY SALVAGE SYSTEM (OSS) TAPER STACKING ADAPTER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LINEAR? 3-4

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 7, 2026

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF SARS-COV-2

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·September 3, 2025

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF SARS-COV-2

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·September 5, 2025

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·November 4, 2015

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·April 29, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·April 20, 2011

    ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT MX2

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·July 25, 2008

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·November 17, 2017

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF SARS-COV-2

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·August 30, 2024

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LIT·May 23, 2016

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012