BEUDAMED
    21 results · 29ms · Sources: EU EUDAMED, US FDA

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    AXIUM DETACHABLE COIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    VACCESS LT LONG-TERM HEMODIALYSIS CATHETER PLUS

    FDA UDI
    Bard Access Systems, Inc.·00801741010897·VACCESS PLUS, ST, 16 FR. 31cm

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1671333100·

    Zavation

    FDA UDI
    Zavation LLC·00197157006136·Sizer with One Stop/0deg/7&8mm

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365105944·

    CRYONIZE TM

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

    REMEEX SYSTEM FOR URINARY INCONTINENCE

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

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144761·L UHMWPE PS Tibial Insert Sz B 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142866·L E-CIMA Vitamin E PS Tibial Insert Sz B 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143726·L CIMA HXL PS Tibial Insert Sz B 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147175·PS Tibia Insert Trial Size B, 10mm - Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172689·PS Tibia Insert Trial with Posterior Pin Relief...

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018

    5.0MM CANNULATED VA LOCKING SCREW/75MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·April 2, 2013

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 29, 2013

    THE EMAX 2 PLUS SYSTEM

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 1, 2014

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·May 12, 2011