MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-05 for PAGEWRITER TC20 CARDIOGRAPH 860332 manufactured by Philips Medical Systems.
[137961861]
A follow-up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
[137961862]
Customer reported screen freezes and they have to restart it constantly. The device was in use on a patient and there was no report of any adverse event.
Patient Sequence No: 1, Text Type: D, B5
[140618345]
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1218950-2019-01729 |
MDR Report Key | 8390813 |
Date Received | 2019-03-05 |
Date of Report | 2019-02-13 |
Date Mfgr Received | 2019-02-13 |
Device Manufacturer Date | 2017-01-18 |
Date Added to Maude | 2019-03-05 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ROBERT CORNING |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786871501 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | PAGEWRITER TC20 CARDIOGRAPH |
Generic Name | PAGEWRITER TC20 CARDIOGRAPH |
Product Code | DPS |
Date Received | 2019-03-05 |
Model Number | 860332 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN ROAD ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-03-05 |