MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-10-29 for ATELLICA CH PHENCYCLIDINE (PCP) 11097509 manufactured by Siemens Healthcare Diagnostics Inc..
Report Number | 2432235-2019-00396 |
MDR Report Key | 9251053 |
Report Source | OTHER |
Date Received | 2019-10-29 |
Date of Report | 2019-10-29 |
Date of Event | 2019-09-19 |
Date Mfgr Received | 2019-10-08 |
Date Added to Maude | 2019-10-29 |
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 | CHRISTINA LAM |
Manufacturer Street | 511 BENEDICT AVE |
Manufacturer City | TARRYTOWN NY 10591 |
Manufacturer Country | US |
Manufacturer Postal | 10591 |
Manufacturer Phone | 9145243504 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
Manufacturer Street | 500 GBC DRIVE PO BOX 6101 REGISTRATION # 2517506 |
Manufacturer City | NEWARK DE 197146101 |
Manufacturer Country | US |
Manufacturer Postal Code | 197146101 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ATELLICA CH PHENCYCLIDINE (PCP) |
Generic Name | ATELLICA CH PHENCYCLIDINE (PCP) |
Product Code | LCM |
Date Received | 2019-10-29 |
Model Number | ATELLICA CH PHENCYCLIDINE (PCP) |
Catalog Number | 11097509 |
Lot Number | 190042 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
Manufacturer Address | 511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-29 |