MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a literature report with the FDA on 2019-11-07 for IMMULITE 2000 XPI ACTH IMMULITE 2000 XPI ACTH manufactured by Siemens Healthcare Diagnostics Products, Limited.
Report Number | 2432235-2019-00402 |
MDR Report Key | 9290144 |
Report Source | LITERATURE |
Date Received | 2019-11-07 |
Date of Report | 2019-11-07 |
Date of Event | 2013-07-19 |
Date Mfgr Received | 2019-10-17 |
Date Added to Maude | 2019-11-07 |
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 | AARTI AZIZ |
Manufacturer Street | 511 BENEDICT AVENUE |
Manufacturer City | TARRYTOWN NY 10591 |
Manufacturer Country | US |
Manufacturer Postal | 10591 |
Manufacturer Phone | 9145242683 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED |
Manufacturer Street | UK REGISTRATION #: 3002806944 GLYN RHONWY |
Manufacturer City | LLANBERIS, LL554EL |
Manufacturer Country | UK |
Manufacturer Postal Code | LL55 4EL |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | IMMULITE 2000 XPI ACTH |
Generic Name | IMMULITE 2000 XPI ACTH |
Product Code | CKG |
Date Received | 2019-11-07 |
Model Number | IMMULITE 2000 XPI ACTH |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED |
Manufacturer Address | GLYN RHONWY LLANBERIS GWYNEDD, LL554EL UK LL55 4EL |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-07 |