BEUDAMED
    38 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 ×

    LINK TrabecuLink Tibial Cones

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    D-10

    FDA UDI
    BIO-RAD LABORATORIES, INC.·00847817003318·D-10 Analytical Cartridge Hemoglobin A1c Program

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·00304040188149·ZIRLUX ML DISC OM2 98x25

    DEBAKEY FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060043·DEBAKEY TISSUE FORCEPS FLAT HANDLE

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180107885·COHEN CANNULA, WITH LARGE/SMALL REMOVABLE ACORN

    Bradshaw Medical Inc.

    FDA UDI
    Bradshaw Medical, Inc.·00810019930140·BIT, HEX MALE 9/64" AO

    NA

    FDA UDI
    G & H Wire Company, Inc.·10190886246580·DISTAL SEGMENT - 19mm MINISCOPE COMPONENT LEFT

    Insurgical, Inc.

    FDA UDI
    Insurgical, Inc.·00850056900102·Sterile Transfer Shield

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180149786·JARCHO CANNULA REPLACEMENT ACORN, RUBBER, PKG OF 3

    PROVEN KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES

    FDA 510(k)
    FDA Class 2 ·Dental

    MEGASYSTEM C

    FDA Adverse Event
    Malfunction ·WALDEMAR LINK GMBH&CO.KG·Product code KRO·July 21, 2023

    DATEX-OHMEDA INC

    FDA Adverse Event
    Other ·DATEX-OHMEDA, INC·Product code CAD·May 22, 2001

    INVERNESS EAR PIERCING SYSTEM

    FDA Adverse Event
    Other ·INVERNESS CORP.·Product code JYS·April 26, 2001

    SEPRAFILM BIORESORBABLE MEMBRANE

    FDA Adverse Event
    Injury ·GENZYME CORPORATION·Product code MCN·October 11, 2001

    PROLIEVE THERMODILITATION SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 15, 2008

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·August 10, 2011

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 1, 2013

    CERTAS PLUS INLINE VALVE ONLY

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·February 27, 2024

    TEMA ELBOW

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JDC·July 26, 2024