BEUDAMED
    16 results · 19ms · Sources: EU EUDAMED, US FDA

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    Disposable Trocars

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

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813034521·K-Type Files 21MM #60

    Azur Pushable Helical

    FDA UDI
    Microvention, Inc.·00810170017445·Azur

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197494526·Micro Forceps 0,5mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197494540·Micro Forceps 0,5mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197494533·Micro Forceps 0,5mm ...

    SpeediCath Compact Set

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

    EAGLE EDGE AXR90 and AXR120

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    aap Implantate AG·04042409445361·Cannulated Headless Bone Screw 2.5, L 20, TL 8 ...

    HUTIV TABLE ASSY STD W/COLOR

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·December 2, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 16, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IOR·July 29, 2013

    Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I

    FDA Enforcement
    Class II ·Completed·Applied Medical Technology Inc·November 19, 2025

    Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 178360 178361 178362 178363 178364 178365 178366 178367 178368 178369 178370 178371 178372 178373 178464 178472 178480 178488 178496 178504 178575 178576 178577 178578 178579 178580 178730 178731 178732 178733 178734 178735 178354S 178754 178755 178756 178757 178758 178759 Product Usage: 1) Correction of revision of unsuccessful osteotomy, arthrodesis or previous joint replacement 2) Tumor resections 3) Revision of previously failed total joint arthroplasty 4) Trauma The ComPreSs Distal Femoral Replacement System is intended for uncemented use.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 60 MM, Silicone, Sterile, Item 432160.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020

    ACCOLADE DR SL MRI (Model L311)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025