FDA Adverse Event Malfunction Summary report: N

HAMILTON-C1

MDR report key: 18180153 · Received November 21, 2023

Report

Report Number
3001421318-2023-03914
Event Type
Malfunction
Date Received
November 21, 2023
Date of Event
October 31, 2023
Report Date
August 17, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002800747
PMA / PMN Number
K181216
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
505

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4). HAMILTON MEDICAL AG COMPLAINT NUMBER: (B)(4). FOLLOW-UP 1 - CORRECTED INFORMATION: **UDI RELATED DATA QUALITY UPDATES ONLY** FIELD D4 WAS UPDATED WITH FULL UDI INFORMATION AS REQUESTED.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4).

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: A CUSTOMER HAS A PROBLEM WITH A COM. BOARD P.N. 161520 S.N. (B)(6): THE NURSE CALL DOESN'T ALERT PROPERLY. NO PATIENT INVOLVEMENT.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: A CUSTOMER HAS A PROBLEM WITH A COM. BOARD P.N. 161520 S.N. (B)(6): THE NURSE CALL DOESN'T ALERT PROPERLY. NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2022048 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDICAL AG 161001 07630002800747

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown