MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other,use report with the FDA on 2019-06-20 for MICROGARD II MICROGUARD V-892392 manufactured by Vyaire Medical.
Report Number | 9615102-2019-00106 |
MDR Report Key | 8719430 |
Report Source | HEALTH PROFESSIONAL,OTHER,USE |
Date Received | 2019-06-20 |
Date of Report | 2019-06-03 |
Date of Event | 2019-02-28 |
Date Mfgr Received | 2019-06-03 |
Date Added to Maude | 2019-06-20 |
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 | CAREFUSION GERMANY 234 GMBH |
Manufacturer Street | LEIBNIZSTRASSE 7 |
Manufacturer City | HOCHBERG, 97204 |
Manufacturer Country | GM |
Manufacturer Postal Code | 97204 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MICROGARD II |
Generic Name | FILTER, BACTERIAL, BREATHING-CIRCUIT |
Product Code | CAH |
Date Received | 2019-06-20 |
Model Number | MICROGUARD |
Catalog Number | V-892392 |
Lot Number | 182415-38 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 1. Other | 2019-06-20 |