MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-21 for MP5 M8105A (865024) manufactured by Philips Medical Systems.
[83304384]
A follow up report will be submitted upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10
[83304385]
The customer reported that there was no local audio. The device was not used for monitoring at the time of the alleged malfunction.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610816-2017-00253 |
MDR Report Key | 6806933 |
Date Received | 2017-08-21 |
Date of Report | 2017-07-27 |
Date Mfgr Received | 2017-07-27 |
Device Manufacturer Date | 2010-04-08 |
Date Added to Maude | 2017-08-21 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. DENYSE MURPHY |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786871501 |
Manufacturer G1 | PHILIPS MEDICAL SYSTEMS |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | MP5 |
Generic Name | PATIENT MONITOR |
Product Code | BZQ |
Date Received | 2017-08-21 |
Model Number | M8105A (865024) |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | HEWLETT-PACKARD STR.2 BOEBLINGEN 71034 GM 71034 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-08-21 |