MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-09 for COCHLEAR OSIA OSI200 IMPLANT N/A manufactured by Cochlear Ltd.
[178311840]
This report is submitted on february 10, 2020.
Patient Sequence No: 1, Text Type: N, H10
[178311841]
Per the clinic, the patient experienced an infection from the patient's glasses rubbing on the wound. The infection was treated with a topical antibiotic.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6000034-2020-00334 |
| MDR Report Key | 9685226 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2020-02-09 |
| Date of Report | 2020-01-17 |
| Date of Event | 2019-11-21 |
| Date Added to Maude | 2020-02-09 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. ROBERTA LOVEDAY |
| Manufacturer Street | 1 UNIVERSITY AVENUE |
| Manufacturer City | MACQUARIE UNIVERSITY, NSW 2109 |
| Manufacturer Country | AS |
| Manufacturer Postal | 2109 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COCHLEAR OSIA OSI200 IMPLANT |
| Generic Name | COCHLEAR? OSIA? SYSTEM |
| Product Code | PFO |
| Date Received | 2020-02-09 |
| Model Number | OSI200 |
| Catalog Number | N/A |
| Lot Number | N/A |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COCHLEAR LTD |
| Manufacturer Address | 1 UNIVERSITY AVENUE MACQUARIE UNIVERSITY, 2109 AS 2109 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-02-09 |