MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-18 for CONFIRM ANTI-SYNAPTOPHYSIN (SP11) RABBIT 05479304001 manufactured by Ventana Medical Systems, Inc..
Report Number | 2028492-2020-00003 |
MDR Report Key | 9850188 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-18 |
Date of Report | 2020-03-18 |
Date of Event | 2020-02-20 |
Date Mfgr Received | 2020-02-20 |
Device Manufacturer Date | 2019-06-05 |
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 | NA STACIE-ANN CREIGHTON |
Manufacturer Street | 1910 E INNOVATION PARK DR NA |
Manufacturer City | TUSCON AZ 85755 |
Manufacturer Country | US |
Manufacturer Postal | 85755 |
Manufacturer Phone | 9082537112 |
Manufacturer G1 | NA |
Manufacturer Street | NA NA |
Manufacturer City | NA |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CONFIRM ANTI-SYNAPTOPHYSIN (SP11) RABBIT |
Generic Name | IMMUNOHISTOCHEMISTRY REAGENTS AND KITS |
Product Code | NJT |
Date Received | 2020-03-18 |
Model Number | NA |
Catalog Number | 05479304001 |
Lot Number | F11948 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VENTANA MEDICAL SYSTEMS, INC. |
Manufacturer Address | 1910 E INNOVATION PARK DR TUCSON AZ 85755 US 85755 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-18 |