FDA Adverse Event Malfunction Summary report: N

HAMILTON-C6

MDR report key: 18063246 · Received November 3, 2023

Report

Report Number
3001421318-2023-03731
Event Type
Malfunction
Date Received
November 3, 2023
Date of Event
October 12, 2023
Report Date
August 12, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002808590
PMA / PMN Number
K201658
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
RP
Reporter Occupation
505

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: SEE (B)(4).

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: SEE CER (B)(4). HAMILTON MEDICAL AG COMPLAINT NUMBER: CER (B)(4). FOLLOW-UP 1 - CORRECTED INFORMATION: **UDI RELATED DATA QUALITY UPDATES ONLY** FIELD D4 WERE UPDATED WITH FULL UDI INFORMATION AS REQUESTED.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: HOSPITAL TECHS REPORTED C6 FAILING SELF TEST AND SHOWING TF CODES 231008 AND 231013.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: HOSPITAL TECHS REPORTED C6 FAILING SELF TEST AND SHOWING TF CODES 231008 AND 231013.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2033222 HAMILTON-C6 HAMILTON-C6 VENTILATOR CBK HAMILTON MEDICAL AG 160021 07630002808590

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown