FDA Adverse Event
Malfunction
Summary report: N
HAMILTON-C1
MDR report key: 18746024
·
Received February 21, 2024
Report
- Report Number
- 3001421318-2024-00420
- Event Type
- Malfunction
- Date Received
- February 21, 2024
- Date of Event
- November 28, 2023
- Report Date
- November 7, 2024
- Manufacturer
- HAMILTON MEDICAL AG
- Product Code
- CBK
- UDI-DI
- 07630002800747
- PMA / PMN Number
- K181216
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- EG
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
Additional Manufacturer Narrative · 0
HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4).
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: DURING START-UP SELF TEST, THE DEVICE SHOWED TE 231022 (PEXPVALVE SENSOR DEFECT). NO PATIENT INVOLVEMENT.
Description of Event or Problem · 0
THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: DURING START-UP SELF TEST, THE DEVICE SHOWED TE 231022 (PEXPVALVE SENSOR DEFECT). NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1670545 | HAMILTON-C1 | HAMILTON-C1 | CBK | HAMILTON MEDICAL AG | 161001 | 07630002800747 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |