MalfunctionOPR
WEB
Received Jul 31, 2026 · Event occurred May 13, 2026
Report 2032493-2026-08110 · MDR key 50106256
Device
Generic name
Intrasaccular Flow Disruption Device
Manufacturer
Microvention, Inc.Model number
W5-5-2-MVI-2Lot number
0001467920
Product problems
- Separation Failure
Patient
Female
- No Clinical Signs, Symptoms or Conditions