FDA Adverse Event Malfunction Summary report: N

HAMILTON-C3

MDR report key: 20084001 · Received August 28, 2024

Report

Report Number
3001421318-2024-02084
Event Type
Malfunction
Date Received
August 28, 2024
Date of Event
July 11, 2024
Report Date
November 19, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002801881
PMA / PMN Number
K201306
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
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.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: INVESTIGATION ONGOING.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: LOSS OF EXTERNAL POWER AND BATTERY NOT CHARGING.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: LOSS OF EXTERNAL POWER AND BATTERY NOT CHARGING.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: LOSS OF EXTERNAL POWER AND BATTERY NOT CHARGING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
197569 HAMILTON-C3 HAMILTON-C3 CBK HAMILTON MEDICAL AG 160005 07630002801881

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown