MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-09-18 for CODMAN DISPOS PERFORATOR 261221 manufactured by Integra Lifesciences Mansfield.
| Report Number | 1226348-2019-00422 |
| MDR Report Key | 9083563 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-09-18 |
| Date of Report | 2019-09-05 |
| Date of Event | 2019-09-04 |
| Date Mfgr Received | 2019-09-05 |
| Date Added to Maude | 2019-09-18 |
| 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 | MRS. KIMBERLY SHELLY |
| Manufacturer Street | 325 PARAMOUNT DRIVE |
| Manufacturer City | RAYNHAM MA 02767 |
| Manufacturer Country | US |
| Manufacturer Postal | 02767 |
| Manufacturer G1 | INTEGRA LIFESCIENCES MANSFIELD |
| Manufacturer Street | 11 CABOT BOULEVARD |
| Manufacturer City | MANSFIELD MA 02048 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 02048 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CODMAN DISPOS PERFORATOR |
| Generic Name | DISPOSABLE PERFORATORS |
| Product Code | HBF |
| Date Received | 2019-09-18 |
| Catalog Number | 261221 |
| Lot Number | J2410W |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INTEGRA LIFESCIENCES MANSFIELD |
| Manufacturer Address | 11 CABOT BOULEVARD 11 CABOT BOULEVARD MANSFIELD MA 02048 US 02048 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-09-18 |