BEUDAMED
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    LINICAL PROTEIN 5 CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER ARRAY AND IMMAGE PROTEIN SYSTEMS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Flex

    FDA UDI
    Diversified Products, Inc.·00037741503026·

    0.6/1.2P366D-150

    FDA UDI
    SHIMADZU CORPORATION·04540217062270·

    BR Surgical, LLC

    FDA UDI
    BR Surgical, LLC·00857556008161·Sinus Scope, autoclavable, Ø 3mm, 30º, 150mm

    BR Surgical, LLC

    FDA UDI
    BR Surgical, LLC·00857556008086·Arthroscope, autoclavable, Ø 3mm, 30º, 150mm

    SCFE Screw

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132114414·4.0mm X 50mm FULL THREAD CANNULATED SCREW

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981174903·Z-Rod, Dia. 5.5mm, Titanium, 150mm

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955934001·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933394·Percutaneous Transluminal Angioplasty Balloon C...

    64 CHANNEL EEG / MODEL NUMBER EX-NW-64

    FDA 510(k)
    FDA Class 2 ·Neurology

    CRC-15BT

    FDA 510(k)
    FDA Class 2 ·Radiology

    8.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV.·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    8.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV.·Product code BTR·September 17, 1999

    9.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    6.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    7.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    9.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999