MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-20 for PK PAPYRUS US 3.5/15 434889 SEE MODEL NO. manufactured by Biotronik Ag, Buelach, Switzerland.
[184274390]
A pk papyrus covered stent system was used to treat a perforation in the lad. Peri-procedural, there was an acute in-stent thrombosis.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1028232-2020-01357 |
| MDR Report Key | 9859997 |
| Report Source | COMPANY REPRESENTATIVE,USER F |
| Date Received | 2020-03-20 |
| Date of Report | 2020-03-18 |
| Date of Event | 2020-02-19 |
| Date Mfgr Received | 2020-03-18 |
| Device Manufacturer Date | 2019-03-19 |
| Date Added to Maude | 2020-03-20 |
| 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 Street | 6024 JEAN ROAD |
| Manufacturer City | LAKE OSWEGO OR 97035 |
| Manufacturer Country | US |
| Manufacturer Postal | 97035 |
| Manufacturer Phone | 8772459800 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PK PAPYRUS US 3.5/15 |
| Generic Name | COVERED CORONARY STENT |
| Product Code | NIV |
| Date Received | 2020-03-20 |
| Model Number | 434889 |
| Catalog Number | SEE MODEL NO. |
| Lot Number | 02196007 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BIOTRONIK AG, BUELACH, SWITZERLAND |
| Manufacturer Address | ACKERSTRASSE 6 BUELACH CH-8180 CH CH-8180 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2020-03-20 |