MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2017-10-12 for LYOPLANT ONLAY 10.0X12.5CM 1067050 manufactured by Aesculap Ag.
[90180398]
(b)(4). Manufacturing site evaluation: evaluation on-going. Device not returned.
Patient Sequence No: 1, Text Type: N, H10
[90180399]
Country of country: usa. It was reportd that after a patient had a grade i meningioma procedure, the patient had a resection of the meningioma. Lyoplant onlay was used at the end of the surgery. Mri reveled a granuloma.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610612-2017-00491 |
| MDR Report Key | 6944050 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2017-10-12 |
| Date of Report | 2017-11-01 |
| Date of Event | 2017-09-15 |
| Date Facility Aware | 2017-09-29 |
| Date Mfgr Received | 2017-09-19 |
| Device Manufacturer Date | 2017-06-24 |
| Date Added to Maude | 2017-10-12 |
| 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. NICOLE BROYLES |
| Manufacturer Street | 615 LAMBERT POINTE DRIVE |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| Manufacturer Phone | 3145515988 |
| Manufacturer G1 | AESCULAP AG |
| Manufacturer Street | PO BOX 40 |
| Manufacturer City | TUTTLINGEN, 78501 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 78501 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LYOPLANT ONLAY 10.0X12.5CM |
| Generic Name | LYOPLANT ONLAY |
| Product Code | MVA |
| Date Received | 2017-10-12 |
| Model Number | 1067050 |
| Catalog Number | 1067050 |
| Lot Number | 216243 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | 3 MO |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AESCULAP AG |
| Manufacturer Address | PO BOX 40 TUTTLINGEN, 78501 GM 78501 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-10-12 |