BEUDAMED
    411 results · 22ms · Sources: EU EUDAMED, US FDA

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    HAMMERLOCK 2

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694035378·3.5mm x 20mm Locking Screw

    SMALL BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919931034·KM33-520

    STILLE Gouges

    FDA UDI
    Stille AB·07332339206673·GOUGE ORIGINAL STILLE 20 mm 21 cm 8.25 in

    CARPENTIER-EDWARDS PHYSIO TRICUSPID ANNULOPLASTY RING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BLUEPHASE

    FDA 510(k)
    FDA Class 2 ·Dental

    Atoll™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981052652·3.5mm x 20mm Smooth Shaft Poly Screw Assm. The ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144860·L UHMWPE PS Tibial Insert Sz C 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143825·L CIMA HXL PS Tibial Insert Sz C 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147274·PS Tibia Insert Trial Size C, 20mm - Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142965·L E-CIMA Vitamin E PS Tibial Insert Sz C 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172849·PS Tibia Insert Trial with Posterior Pin Relief...

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 29, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 20, 2011

    STONETOME STONE REMOVAL DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FDI·August 22, 2008

    U-BLADE SET, TI GAMMA3 10.5X100MM

    FDA Adverse Event
    Injury ·STRYKER OSETOSYNTHESIS KIEL·Product code HSB·December 18, 2012

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 19, 2026

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 9, 2022

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 30, 2026

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 6, 2025