MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE ECHO-HD-22-EBUS-O manufactured by Cook Ireland Ltd.
| Report Number | 3001845648-2020-00172 |
| MDR Report Key | 9902164 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2020-03-31 |
| Date of Report | 2020-03-02 |
| Date of Event | 2020-02-19 |
| Date Facility Aware | 2020-02-19 |
| Date Mfgr Received | 2020-03-02 |
| Device Manufacturer Date | 2019-09-30 |
| Date Added to Maude | 2020-03-31 |
| 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 | MS. HEATHER RYAN |
| Manufacturer Street | O HALLORAN ROAD NATIONAL TECHNOLOGY PARK |
| Manufacturer City | LIMERICK |
| Manufacturer G1 | COOK IRELAND LTD |
| Manufacturer Street | O HALLORAN ROAD NATIONAL TECHNOLOGY PARK |
| Manufacturer City | LIMERICK |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE |
| Generic Name | FCG KIT, NEEDLE, BIOPSY |
| Product Code | FCG |
| Date Received | 2020-03-31 |
| Returned To Mfg | 2020-03-10 |
| Catalog Number | ECHO-HD-22-EBUS-O |
| Lot Number | CF1654773 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | 142 DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK IRELAND LTD |
| Manufacturer Address | O HALLORAN ROAD LIMERICK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-31 |