FDA Adverse Event Malfunction Summary report: N

SAPPHIRE M.T INFUSION PUMP - FRENCH

MDR report key: 21813612 · Received April 10, 2025

Report

Report Number
3010293992-2025-00029
Event Type
Malfunction
Date Received
April 10, 2025
Date of Event
March 30, 2025
Report Date
April 22, 2025
Manufacturer
EITAN MEDICAL LTD.
Product Code
FRN
UDI-DI
7290109150710
PMA / PMN Number
K192860
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
BIOMEDICAL ENGINEER
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS REPORTED EVENT OCCURRED OUTSIDE OF THE US ON A DEVICE THAT IS SIMILAR TO THE ONE MARKETED IN THE US AND FOR WHICH THERE IS NO DATA IN GUDID. DEVICE'S PREMARKET SUBMISSION NUMBER: K192860.

Additional Manufacturer Narrative · 0

THIS REPORTED EVENT OCCURRED OUTSIDE OF THE US ON A DEVICE THAT IS SIMILAR TO THE ONE MARKETED IN THE US AND FOR WHICH THERE IS NO DATA IN GUDID. DEVICE'S PREMARKET SUBMISSION NUMBER: K192860.

Description of Event or Problem · 0

THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM FRANCE. DELIVERY ISSUE.

Description of Event or Problem · 0

THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM FRANCE. DELIVERY ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
415480 SAPPHIRE M.T INFUSION PUMP - FRENCH INFUSION PUMP FRN EITAN MEDICAL LTD. 7290109150710

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown