BEUDAMED
    9 results · 28ms · 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 ×

    S.I.N. Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    Brisbane ALIF Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215018214·

    ORTHOPEDIC WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEFEND Ear-loop Face Masks

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

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·HITACHI HIGH TECH CORP.·Product code JJE·November 12, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 26, 2011

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 17, 2013

    Aquapak 340 SW, 340, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·July 16, 2014

    Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication.

    FDA Enforcement
    Class II ·Terminated·Unomedical As·July 1, 2015