FDA Adverse Event Malfunction Summary report: N

SAPPHIRE INFUSION PUMP- ENGLISH

MDR report key: 12849865 · Received November 21, 2021

Report

Report Number
3010293992-2021-00057
Event Type
Malfunction
Date Received
November 21, 2021
Date of Event
October 28, 2021
Report Date
December 21, 2021
Manufacturer
EITAN MEDICAL LTD
Product Code
FRN
PMA / PMN Number
K192860
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

EITAN MEDICAL LTD IS FORMERLY NAMED Q CORE MEDICAL LTD. (B)(4).

Additional Manufacturer Narrative · 0

EITAN MEDICAL LTD IS FORMERLY NAMED Q CORE MEDICAL LTD. THE FEI NUMBER IS THE SAME (B)(4).

Additional Manufacturer Narrative · 0

EITAN MEDICAL LTD IS FORMERLY NAMED Q CORE MEDICAL LTD. THE FEI NUMBER IS THE SAME (B)(4).

Description of Event or Problem · 0

THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM (B)(6): DELIVERY ISSUE.

Description of Event or Problem · 0

THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM (B)(6) : DELIVERY ISSUE.

Description of Event or Problem · 0

THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM (B)(6): DELIVERY ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1747857 SAPPHIRE INFUSION PUMP- ENGLISH INFUSION PUMP FRN EITAN MEDICAL LTD

Patients

Seq Age Sex Outcome Treatment
1 Unknown