Brand Name | VMAX |
Type of Device | CALCULATOR, PREDICTED VALUES, PULMONARY FUNCTION |
Manufacturer (Section D) |
VYAIRE MEDICAL |
22745 savi ranch pkwy |
yorba linda CA 92887 |
|
Manufacturer (Section G) |
VYAIRE MEDICAL INC. |
1100 bird center drive |
|
palm springs CA 92262 |
|
Manufacturer Contact |
stanley
tan
|
22745 savi ranch pkwy |
yorba linda, CA 92887
|
7149193324
|
|
MDR Report Key | 8713841 |
MDR Text Key | 148474182 |
Report Number | 2021710-2019-10389 |
Device Sequence Number | 1 |
Product Code |
BTY
|
UDI-Device Identifier | 10846446021417 |
UDI-Public | (01)10846446021417(11)20060601 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K942211 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional,user faci |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
11/19/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 06/19/2019 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | VMAX ENCORE 22D |
Device Catalogue Number | 777405-101 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 11/19/2018 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 06/01/2006 |
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) |
Other;
|