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

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    PENTRA 80

    FDA 510(k)
    FDA Class 2 ·Hematology

    PureGuard

    FDA UDI
    PURELIFE, LLC·D79010240021·Small, Soft, nitrile powder-free, Textured fing...

    NA

    FDA UDI
    Stryker GmbH·00886385006499·Carpal Fusion Plate, Small

    FPS

    FDA UDI
    Tyber Medical, LLC·00810040688812·Cartilage removal tool, 14mm

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0140020·Driver Shaft, T30 No Taper, Final Cap Driver

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0140020·Driver Shaft, T30 Final Cap, MIS

    ePatch electrode-patch

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146EPE30·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197470834·Farrior Aural Speculum, round Ø 6.5m...

    IMMULITE CK-MB, MODEL LKMB1 (100 TESTS), LKMB5 (500 TESTS); IMMULITE 2000 CK-MB, MODEL L2KMB2 (200 TESTS), L2KMB6 (600)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    P4200,S800, 24" - 680+,790,PS BREAKAWAY

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828183574·P4200,S800, 24" - 680+,790,PS BREAKAWAY

    800 DIN CORD SAVER,EXT CBL, 24",CURB

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828129343·800 DIN CORD SAVER,EXT CBL, 24",CURB

    KL 1.8 FIBERTAK, SHOULDER

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·October 16, 2023

    ZIMMER ZIRCONIA FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWY·September 18, 2009

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MND·March 27, 2013

    SYSTEM 5 SAGITTAL SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·February 14, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP.

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 4, 2008

    THREE PEG PATELLA 32MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 11, 2025

    THREE PEG PATELLA 32MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 27, 2025

    ONE PEG PATELLA 32MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 3, 2025