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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    rainbow CT

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777631·LUMBAMED BASIC DORSAL STAYS M SILVER I

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694091022·Profile Plus VisiDisk

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776373078·VOLKMAN RETRACTOR 3 PRONG SHARP

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114254·CHAMBER MAINTAINER 25GA (PK/10)

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319742549·Freer Submucous Chisel 6-1/2" (16.3cm), curved,...

    BALANCE MICROPLASTY BROACH

    FDA UDI
    Biomet Orthopedics, LLC·00880304458840·

    ACRA-CUT

    FDA UDI
    ACRA-CUT INC·00810607002716·Disposable Cranial Perforator

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780380566·Integra® Jarit® Volkman Retractor, 8-1/2", 3 Pr...

    ACRA-CUT

    FDA Adverse Event
    Malfunction ·ACRA-CUT INC.·Product code HBF·June 30, 2010

    LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HARDYDISK, SULFA/TRIMETH

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ACRA-CUT

    FDA Adverse Event
    Malfunction ·ACRA CUT, INC·Product code HBF·April 10, 2025

    Disposable Cranial Perforator

    FDA UDI
    ACRA-CUT INC·00810607000071·Cranial Perforator

    PRIMA TT GLENOID

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MBF·November 6, 2025

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 1, 2016

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH PRE-ATTACHED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·January 31, 2024

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    PIONEER PLUS CATHETER

    FDA Adverse Event
    Malfunction ·Product code PDU·October 22, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·July 1, 2013