FDA Adverse Event Injury Summary report: N

PROSESNE CRYOABLATION SYSTEM

MDR report key: 23757016 · Received December 9, 2025

Report

Report Number
3008797959-2025-00011
Event Type
Injury
Date Received
December 9, 2025
Date of Event
November 13, 2025
Report Date
November 13, 2025
Manufacturer
ICECURE MEDICAL LTD
Product Code
GEH
UDI-DI
07290015487160
PMA / PMN Number
K183213
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PL
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

RECURRENCE AFTER CRYOABLATION TREATMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2722545 PROSESNE CRYOABLATION SYSTEM GEH ICECURE MEDICAL LTD FAS3100000 07290015487160

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other