BEUDAMED
    21 results · 24ms · Sources: EU EUDAMED, US FDA

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    COLLAGEN DENTAL MENBRANE - CONFORMABLE II

    FDA 510(k)
    FDA Class 2 ·Dental

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111151309·SURG SCRUB BRUSH STANDARD

    VENTILATOR, CONTINUOUS (RESPIRATOR), MODEL LTV 1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    C3 ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G2 FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 21, 2007

    RECOVERY G2 FILTER SYSTEM, FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 23, 2007

    G2 FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 19, 2010

    SPARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·April 12, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 19, 2011

    TRAPEASE PERMANENT VENA CAVA FILTER 55 CM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code DQO·June 18, 2008

    RECOVERY G2 FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·February 5, 2010

    G7 PPS LTD ACET SHELL 56F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 11, 2024

    RECOVERY G2 FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·September 15, 2009

    G2 FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·September 21, 2007

    TAPERLOC TPRLC 133 T1 PPS SO 14X148MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·March 11, 2024

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·November 4, 2021

    G7 LONGEVITY NEUTRAL 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 11, 2024

    RECOVERY G2 FILTER SYSTEM, FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 27, 2007

    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

    CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015