BEUDAMED
    35 results · 26ms · 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 ×

    QUINUPRISTIN/DALFOPRISTIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Essential Kit

    FDA UDI
    MEDIVATORS INC.·40677964008366·Essential Kit includes Brush, DEFENDO Air/Water...

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741188053·Catheter Placement Kit

    TASMIN R 0°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844014325·The basic shape of the TASMIN R devices is a ho...

    Deploy™ Expandable Interbody System

    FDA UDI
    Southern Spine LLC·00815351022232·Lumbar Expandable Cage, 0 Degree, 28mm Length, ...

    RENAFLO II HF 2000 HEMOFILTER

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

    HARDYDISK, CEFAZOLIN, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PORTEX TUBES BLUSELECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 6, 2022

    PORTEX TUBES BLUSELECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 7, 2022

    PORTEX BLUSELECT TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 29, 2022

    LOCKING CORTICAL/CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·September 9, 2013

    LOCKING CORTICAL/CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·September 9, 2013

    LOCKING CORTICAL/CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·September 9, 2013

    LOCKING CORTICAL/CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·September 9, 2013

    LOCKING CORTICAL/CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·September 9, 2013

    UCSS SCREW SET

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MRW·June 4, 2009

    UCSS SCREW SET

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code HWC·June 4, 2009

    PORTEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·March 8, 2022

    PORTEX BLUE LINE ULTRA SUCTIONAID

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 28, 2022

    PORTEX TUBES BLUSELECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTC·January 7, 2022