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

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    PRO-TOE VO HAMMERTOW IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Preci-Bar

    FDA UDI
    Preat Corporation·00842092155332·Preci-Bar Standard (Resilient) Plastic Bar (4-P...

    MegaBeam® Reusable Fiber Optic Delivery System

    FDA UDI
    Ceram Optec SIA·04049089100429·

    DD Bio Splint P

    FDA UDI
    Dental Direkt GmbH·EDDIK101151·DD Bio Splint P are transparent dental milling ...

    DOYEN KOCHER INTESTINAL FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896101449·DOYEN KOCHER INTESTINAL FORCEPS CURVED LONGITUD...

    S-Core™

    FDA UDI
    SUBCHONDRAL SOLUTIONS, INC.·00850017962392·Size 6 Cannulated Sizer

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161011650·Alignment Rod

    Micro Milling Drum XXF

    FDA UDI
    Spierings Orthopaedics B.V.·08720828234037·

    Zavation

    FDA UDI
    Zavation LLC·00197157009762·6.5mm TAP, CANNULATED

    POWDER-FREE, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEPF1

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POLYMER COATED POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NY-STA BLACK 2/0 18" (45CM) DS24 VPL

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026

    ELLIPSE DR, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·May 24, 2011

    DELTEC COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code LZG·August 5, 2008

    SUPRAMID BLACK 3/0 (2) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023

    UNK HAKIM

    FDA Adverse Event
    Injury ·Product code JXG·November 21, 2017

    SKIN SUTURE PACK DAFILON

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 18, 2024

    SUPRAMID BLACK 4/0 (1.5) 45CM DS16

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 17, 2025