MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-25 for PROGRESSIVE MEDICAL PMI OPERATIVE CHOLANGIOGRAM CATH PMIORCA-2-REV.0 REORDER: PMORCA manufactured by Unk.
Report Number | MW5090062 |
MDR Report Key | 9124480 |
Date Received | 2019-09-25 |
Date of Report | 2019-09-23 |
Date of Event | 2019-09-21 |
Date Added to Maude | 2019-09-26 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | PROGRESSIVE MEDICAL PMI OPERATIVE CHOLANGIOGRAM CATH |
Generic Name | CATHETER, CHOLANGIOGRAPHY |
Product Code | GBZ |
Date Received | 2019-09-25 |
Model Number | PMIORCA-2-REV.0 |
Catalog Number | REORDER: PMORCA |
Lot Number | 014190301 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | UNK |
Manufacturer Address | UNK UNK |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-25 |