BEUDAMED
    28 results · 24ms · 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 ×

    DISPOSABLE SPETZLER-MALIS DUAL IRRIGATING BIPOLAR FORCEPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821109240·FORCEPS, DRESSING, DENTAL

    TETRIS 0°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844001400·The basic shape of the KIMBA®, KIMBA® mini, MOB...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306819520·Deaver Blade Large 2" x 5"

    Posted Stainless Steel Archwire

    FDA UDI
    Ortho Arch Company Inc·D90911092414·.019 X .025 POSTED SS RIGHT FORM WIRES 24MM (10)

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P11092470·11mm PLIF Implant 9mm Wide 24mm Length, 7 deg L...

    MODIFICATION TO PLUM XL INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FETAL DOPPLER JPD-100S

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    XCELA POWER INJECTABLE PLASTIC TITANIUM PORT

    FDA Adverse Event
    Malfunction ·PFM MEDICAL, INC·Product code LJT·December 18, 2012

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 4, 2022

    CAIMAN DISP. INSTR. NON ARTICUL.D:5 / 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/ 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·February 27, 2015

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 8, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 2, 2011