BEUDAMED
    40 results · 20ms · Sources: EU EUDAMED, US FDA

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    ANTI-SNORING DEVICE OR ASD

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526780750·LEVAMED ACTIVE ANKLE SUP SLVR L III

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189720·LEVAMED ACTIVE ANKLE SUP BLACK L III

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0112230·Tap, 5.50mm, Cannulated, Fixed Sleeve

    VerteGlide Spinal Growth Guidance System

    FDA UDI
    ORTHOPEDIATRICS CORP.·00840194479981·VERTEGLIDE 5.5mm MANUAL COUNTER TORQUE TUBE

    VerteGlide Spinal Growth Guidance System

    FDA UDI
    ORTHOPEDIATRICS CORP.·00840194480031·5.5 OPEN VERTEGLIDE PEDICLE SCREW DRIVER

    VerteGlide Spinal Growth Guidance System

    FDA UDI
    ORTHOPEDIATRICS CORP.·00840194480215·5.5MM PROVISIONAL ROD

    VerteGlide Spinal Growth Guidance System

    FDA UDI
    ORTHOPEDIATRICS CORP.·00840194480208·VERTEGLIDE 5.5MM ROD BEND CHECKER

    D.SIGN 96

    FDA 510(k)
    FDA Class 2 ·Dental

    COOL-TEC ELECTRODES

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

    TROCAR

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS, INC.·Product code DYB·June 5, 2018

    MAXCEM ELITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·March 19, 2013

    INTRALASE FEMTOSECOND LASER

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA LLC·Product code HNO·March 4, 2011

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·March 11, 2008

    REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 75, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·April 26, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·May 6, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 26/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 26, 2019

    REVITAN, PROXIMAL PART, CYLINDRICAL, UNCEMENTED, 65, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 20/200

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·February 13, 2019