MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2020-03-27 for RUSCH EQUIPLED BLADEMAC 3 5843 manufactured by Teleflex Medical.
| Report Number | 8030121-2020-00078 |
| MDR Report Key | 9891898 |
| Report Source | DISTRIBUTOR,FOREIGN |
| Date Received | 2020-03-27 |
| Date of Report | 2020-03-25 |
| Date of Event | 2020-02-19 |
| Date Mfgr Received | 2020-03-25 |
| Date Added to Maude | 2020-03-27 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | VICTORIA SANDLIN |
| Manufacturer Street | 3015 CARRINGTON MILL BLVD |
| Manufacturer City | MORRISVILLE NC 27560 |
| Manufacturer Country | US |
| Manufacturer Postal | 27560 |
| Manufacturer G1 | TRUPHATEK INTERNATIONAL LTD. |
| Manufacturer Street | 14 BENNY GAON STREET P.O. 8051 |
| Manufacturer City | NETANYA 4250443 |
| Manufacturer Country | IS |
| Manufacturer Postal Code | 4250443 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RUSCH EQUIPLED BLADEMAC 3 |
| Generic Name | LARYNGOSCOPE, RIGID |
| Product Code | CCW |
| Date Received | 2020-03-27 |
| Catalog Number | 5843 |
| Lot Number | 180601 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL |
| Manufacturer Address | ATHLONE |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-27 |