BEUDAMED
    29 results · 38ms · 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 ×

    VERSA-DIAL HUMERAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TESS GLENOID REVERSE HEAD DIAMETER 36

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016

    Kirschner w.trocar point, d/e 1.1mm/15cm

    FDA UDI
    mahe medical gmbh·EMAH00406100110·Kirschner w.trocar point, d/e 1.1mm/...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659208667·Kirschner w.trocar point,d/e,2.0mm/15cm _x000D_...

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106100·Trial, 26 x 10mm, 8 Degree, Tapered, Straight

    Kirschner w.trocar point,d/e,2.0mm/15cm

    FDA UDI
    mahe medical gmbh·EMAH00406100200·Kirschner w.trocar point,d/e,2.0mm/15cm

    Kirschner w.trocar point, d/e 1.2mm/15cm

    FDA UDI
    mahe medical gmbh·EMAH00406100120·Kirschner w.trocar point, d/e 1.2mm/...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659208605·Kirschner w.trocar point, d/e _x000D_...

    Kirschner w.trocar point,d/e,1.6mm/15cm

    FDA UDI
    mahe medical gmbh·EMAH00406100160·Kirschner w.trocar point,d/e,1.6mm/15cm

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659208582·Kirschner w.trocar point, d/e _x000D_...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659208575·Kirschner w.trocar point, d/e _x000D_...

    Kirschner w.trocar point, d/e 1.4mm/15cm

    FDA UDI
    mahe medical gmbh·EMAH00406100140·Kirschner w.trocar point, d/e 1.4mm/...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659208629·Kirschner w.trocar point,d/e,1.6mm/15cm _x000D_...

    B-P TOTAL SHOULDER SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193025456·B-P SHOULDER SALVAGE HUMERAL STEM W/ BIOCOAT & ...

    RAPID EXCHANGE BIOPSY CAP AND LOCKING DEVICE #4526 & 4527

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

    RESOLUTION CHOLESTEROL MONITOR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Pneumosure

    FDA UDI
    STRYKER CORPORATION·07613327063295·XL High Flow Insufflator

    FLEXIVA (TM) ID HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·February 25, 2021

    SINGLE USE ELECTROSURGICAL KNIFE KD-655

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 21, 2025

    SUNBEAM

    FDA Adverse Event
    Malfunction ·SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTION·Product code KFZ·March 13, 2013