MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2018-08-21 for INTELLISPHERE EVENT MANAGEMENT 866030 manufactured by Philips Medical Systems.
[117700403]
A follow up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
[117700404]
The customer reported that the emergency display no longer shows any alarms. There was no patient incident.
Patient Sequence No: 1, Text Type: D, B5
[140019324]
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1218950-2018-06734 |
MDR Report Key | 7800521 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2018-08-21 |
Date of Report | 2018-07-25 |
Date Mfgr Received | 2018-07-25 |
Device Manufacturer Date | 2018-06-11 |
Date Added to Maude | 2018-08-21 |
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 | MS. BETTY HARRIS |
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 | 3 |
Brand Name | INTELLISPHERE EVENT MANAGEMENT |
Generic Name | COMMUNICATION SYSTEM |
Product Code | MSX |
Date Received | 2018-08-21 |
Model Number | 866030 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
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 | 2018-08-21 |