FDA Adverse Event Malfunction Summary report: N

HAMILTON-C1

MDR report key: 19869963 · Received July 31, 2024

Report

Report Number
3001421318-2024-01814
Event Type
Malfunction
Date Received
July 31, 2024
Date of Event
June 25, 2024
Report Date
October 25, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002800747
PMA / PMN Number
K181216
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UP
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4). FOLLOW-UP 1 - CORRECTED INFORMATION: **UDI RELATED DATA QUALITY UPDATES ONLY** FIELD D4 WAS UPDATED WITH FULL UDI INFORMATION. UPDATED FIELDS: B4, D4, G6, H2, H4, H11.

Additional Manufacturer Narrative · 0

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

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: AFTER STARTUP, SELFTEST FAILED. TE 233001 (PVENT_MONITOR AUTOZERO FAILED), 233005, 232002 (PVENT_MONITOR DEFECT). NO PATIENT INVOLVEMENT.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: AFTER STARTUP, SELFTEST FAILED. TE 233001 (PVENT_MONITOR AUTOZERO FAILED), 233005, 232002 (PVENT_MONITOR DEFECT). NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1776598 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDICAL AG 161001 07630002800747

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown