BEUDAMED
    334 results · 33ms · 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 ×

    BIPOLAR FORCEPS

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

    ihcDirect® Pan-CK 4Abs

    FDA UDI
    NOVODIAX, INC.·00850000596214·Clones AE1/AE3, C94, R226

    Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L58mm

    FDA UDI
    Laboratoires Bodycad Inc·00688346002850·Button Head Locking HA 4.5 Cortical Self Tappin...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166602·Initia T3 Acetabular Hemispherical Shell, Multi...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523106301·Porous Acetabular Cup System - Hemispherical Sh...

    URETRON MODEL URT

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

    CORD STICK MULTIPLE DRAW SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    MEDICHOICE

    FDA Adverse Event
    Injury ·DALIAN GOODWOOD MEDICAL CARE LTD.·Product code KXF·May 23, 2013

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021