BEUDAMED
    44 results · 23ms · 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 ×

    COLORED POWDER FREE AND POLYMER COATED EXAMINATION GLOVE (BLUE, BLACK AND PINK) WITH A PROTEIN CLAIM OF LESS THAN

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Oticon

    FDA UDI
    Oticon A/S·05707131164018·ACTO, BTE 13 SGR

    ILIZAROV

    FDA UDI
    Smith & Nephew, Inc.·03596010029690·SLOTTED FIXATION BOLT - SMALL BONE FIXATOR

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331186691·mayo vein stripper, 15 3/8" (39.0 cm), 9.6 mm i...

    DEBAKEY AORTIC ANEURYSM CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896003064·DEBAKEY AORTIC ANEURYSM CLAMP CURVED JAW REVERS...

    DEBAKEY AORTIC ANEURYSM CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921006940·DEBAKEY AORTIC ANEURYSM CLAMP CURVED JAW REVERS...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450727874·

    simex

    FDA UDI
    SIMEX Medizintechnik GmbH·04052262385568·SIMEX200 NPWT-System, green

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494461866·Cup Forceps Straight Jaw D 3.0mm, WL 260mm

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964101502·Endo Carry-On Procedure Kit

    PRECISION THIN (9.0 X 0.38 X 25.0MM)

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFA·June 8, 2021

    INCLUDER CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PECTOFIX DYNAMIC STERNAL FIXATION SYSTEM (DSF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2.4MM VA LOCKING SCREW STARDRIVE 22MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 25, 2013

    VA LOCKSCR Ø2.4 SELF-TAP L18 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HRS·July 15, 2013

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 24, 2015

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·May 8, 2013

    ACTIVELIFE 1 PC DRAINABLE POUCH W/ STOMAHESIVE

    FDA Adverse Event
    Injury ·CONVATEC, INC.·Product code EZQ·September 12, 2014

    2.4MM TI LOCKING SCR SLF-TPN WITH STARDRIVE RECESS 18MM

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HWC·June 21, 2017

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·December 24, 2015