MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-11-26 for VMAX ENCORE 22D E 777405-103 manufactured by Vyaire Medical.
Report Number | 2021710-2019-11066 |
MDR Report Key | 9375957 |
Report Source | DISTRIBUTOR,FOREIGN |
Date Received | 2019-11-26 |
Date of Report | 2019-10-31 |
Date of Event | 2019-10-31 |
Date Mfgr Received | 2019-10-31 |
Device Manufacturer Date | 2019-05-08 |
Date Added to Maude | 2019-11-26 |
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 | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | STANLEY TAN |
Manufacturer Street | 22745 SAVI RANCH PKWY |
Manufacturer City | YORBA LINDA CA 92887 |
Manufacturer Country | US |
Manufacturer Postal | 92887 |
Manufacturer Phone | 7149193324 |
Manufacturer G1 | VYAIRE MEDICAL INC. |
Manufacturer Street | 1100 BIRD CENTER DRIVE |
Manufacturer City | PALM SPRINGS CA 92262 |
Manufacturer Country | US |
Manufacturer Postal Code | 92262 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VMAX ENCORE |
Generic Name | CALCULATOR, PREDICTED VALUES, PULMONARY FUNCTION |
Product Code | BTY |
Date Received | 2019-11-26 |
Model Number | 22D E |
Catalog Number | 777405-103 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VYAIRE MEDICAL |
Manufacturer Address | 22745 SAVI RANCH PKWY YORBA LINDA CA 92887 US 92887 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-26 |