InjuryPLJ
LIQUIFIX FIX8
Received Jan 13, 2025
Report 9617175-2025-00002 · MDR key 21136776
Device
Generic name
Hernia Mesh Fixation
Manufacturer
Advanced Medical Solutions (plymoiuth) LtdModel number
72014032Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Hernia
- Hernia
Narrative
Additional Manufacturer Narrative
PATIENT DEATAILS WERE NOT PROVIDED FROM THE REPORTER. INFOMRATION IS LIMITED AS THIS IS REPORTED THIRD PARTY VIA A REGISTRY.
Description of Event or Problem
ACCORDING TO THE REPORT DURING THE INTERIM PROGRESS REPORT OF OUR US CLINICAL STUDY HERNIA RECURRENCE REQUIRING RE-OPERATION. TIME: WITHIN 30D OF SURGERY. DEVICE: LIQUIFIX FIX8 72014032. AS IT IS REPORTED VIA A REGISTRY, SPECIFIC PATIENT DETAILS AND/OR SITE WAS NOT REPORTED. EXCEPT THAT IT IS IN THE USA AND IT IS THE LIQUIFIX FIX8 72014032 DEVICE.