FDA Adverse Event Malfunction Summary report: N

HAMILTON-C6

MDR report key: 18604441 · Received January 30, 2024

Report

Report Number
3001421318-2024-00226
Event Type
Malfunction
Date Received
January 30, 2024
Date of Event
January 19, 2024
Report Date
November 18, 2025
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002808590
PMA / PMN Number
K201658
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: INVESTIGATION ONGOING.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: INVESTIGATION ONGOING. HAMILTON MEDICAL AG COMPLAINT NUMBER: (B)(4).

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: VENTILATOR SWITCHED ITSELF INTO STANDBY.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: VENTILATOR SWITCHED ITSELF INTO STANDBY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1043232 HAMILTON-C6 HAMILTON-C6 VENTILATOR CBK HAMILTON MEDICAL AG 160021 07630002808590

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown