BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    FIBER OPTIC LIGHT SOURCE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209120338·KIT, ETAK - ADVANCED - BLK

    DISPOSABLE MICROKERATOME BLADES-PE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    FLOCHANNEL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·September 29, 1998

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 8, 2014

    SCULPTRA (POLY-L-LACTIC ACID)

    FDA Adverse Event
    Injury ·AVENTIS PHARMA GRUPPO LEPETIT S.R.L.·Product code LMH·October 17, 2012

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 11, 2010

    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

    paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·October 2, 2024

    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·March 27, 2024