MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-18 for VIDAS? MEASLES IGG 30219 manufactured by Biomerieux Sa.
Report Number | 8020790-2020-00025 |
MDR Report Key | 9847905 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2020-03-18 |
Date of Report | 2020-03-18 |
Date Mfgr Received | 2020-02-17 |
Device Manufacturer Date | 2019-05-10 |
Date Added to Maude | 2020-03-18 |
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 | MS. JENNIFER ARMSTRONG |
Manufacturer Street | 595 ANGLUM ROAD |
Manufacturer City | HAZELWOOD, MO |
Manufacturer Country | US |
Manufacturer Phone | 5068201 |
Manufacturer G1 | BIOMERIEUX SA |
Manufacturer Street | 376 CHEMIN DE L ORME |
Manufacturer City | MARCY L ETOILE, 69280 |
Manufacturer Country | FR |
Manufacturer Postal Code | 69280 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VIDAS? MEASLES IGG |
Generic Name | VIDAS? MEASLES IGG |
Product Code | LJB |
Date Received | 2020-03-18 |
Model Number | 30219 |
Catalog Number | 30219 |
Lot Number | 1007322860 |
Device Expiration Date | 2020-03-25 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMERIEUX SA |
Manufacturer Address | 376 CHEMIN DE L ORME MARCY L ETOILE, 69280 FR 69280 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-18 |