BEUDAMED
    10,000 results · 43ms · 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 ×

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897203·NT OPEN COIL VARIABLE FORCE SPRING .012X.030 7 ...

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897227·NT OPEN COIL CONSTANT FORCE SPRING .010X.030 15...

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897234·NT OPEN COIL CONSTANT FORCE SPRING .010X.045 1...

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897241·NT OPEN COIL VARIABLE FORCE SPRING .012X.030 15...

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897180·NT OPEN COIL CONSTANT FORCE SPRING .010X.045 7 ...

    Phoenix Nickel Titanium

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772897166·NT OPEN COIL CONSTANT FORCE SPRING .010X.030 7 ...

    Halyard

    FDA UDI
    O&M HALYARD, INC.·10680651947281·HALYARD* Thermal Pad - Split Torso-5 ft. 3 in. ...

    Halyard

    FDA UDI
    O&M HALYARD, INC.·10680651947274·HALYARD* Thermal Pad, Split Torso, Small

    Halyard

    FDA UDI
    O&M HALYARD, INC.·10680651947298·HALYARD* Thermal Pad - Split Torso Large

    CELL-DYN HEMOGLOBIN/NOC LYSE

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·May 4, 2011

    SUB-Q PORT PERITON (NO C

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·July 24, 2019

    SUB-Q PORT PERITON (NO C

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·July 17, 2019

    SALINE FLUSHES

    FDA Adverse Event
    MEDEFIL, INC.·Product code NZW·January 28, 2022

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 18, 2017

    CELL-DYN RUBY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·March 31, 2025

    HAMILTON-G5

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 19, 2024

    FLOWFLEX COVID-19 ANTIGEN HOME TEST

    FDA Adverse Event
    Malfunction ·ACON LABORATORIES, INC.·Product code QKP·May 14, 2026

    BLUNT FILL SYRINGE

    FDA Adverse Event
    Other ·BD·Product code FMF·April 10, 2024

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·December 28, 1997

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 24, 2015