Brand Name | 3100 HIGH FREQUENCY OSCILLATORY VENTILATOR (HFOV) |
Type of Device | VENTILATOR, HIGH FREQUENCY |
Manufacturer (Section D) |
VYAIRE MEDICAL, INC |
22745 savi ranch parkway |
yorba linda CA 92887 |
|
Manufacturer (Section G) |
VYAIRE MEDICAL, INC |
cerrada via de la produccion |
no. 85., parque industrial mex |
mexicali baja california norte |
MX
|
|
Manufacturer Contact |
kristin
graf
|
22745 savi ranch parkway |
yorba linda, CA 92887
|
|
MDR Report Key | 7332839 |
MDR Text Key | 102181944 |
Report Number | 2021710-2018-07527 |
Device Sequence Number | 1 |
Product Code |
LSZ
|
Combination Product (y/n) | N |
Reporter Country Code | SF |
PMA/PMN Number | P890057 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
distributor,foreign |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
03/12/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/12/2018 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | FISHER & PAYKEL MR730 HUMIDIFIER FLEXIBLE CIRCUIT WITH LONG HEATED WIRE |
Device Catalogue Number | 771375 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 02/12/2018 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|