inforMED
MalfunctionDTB

FINELINE II Sterox

Received Jul 30, 2026 · Event occurred Jun 21, 2026

Report 2124215-2026-40847 · MDR key 50081885

Device

Generic name

Implantable Lead

Model number

4457

Catalog number

4457

Product problems

  • Signal Artifact/Noise
  • Over-Sensing

Patient

Unknown

  • No Clinical Signs, Symptoms or Conditions