MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-08 for C8401, S ALEXIS O WND PROT/RET 5/BX 101356101 manufactured by Applied Medical Resources.
| Report Number | 2027111-2019-00550 |
| MDR Report Key | 8876933 |
| Date Received | 2019-08-08 |
| Date of Report | 2019-09-03 |
| Date of Event | 2019-06-26 |
| Date Mfgr Received | 2019-07-12 |
| Device Manufacturer Date | 2019-04-10 |
| Date Added to Maude | 2019-08-08 |
| 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 | WENDY KOBAYASHI |
| Manufacturer Street | 22872 AVENIDA EMPRESA |
| Manufacturer City | RANCHO SANTA MARGARITA CA 92688 |
| Manufacturer Country | US |
| Manufacturer Postal | 92688 |
| Manufacturer Phone | 9497138059 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | C8401, S ALEXIS O WND PROT/RET 5/BX |
| Generic Name | PROSTHESIS, FINGER, CONSTRAINED, METAL/POLYMER |
| Product Code | KGW |
| Date Received | 2019-08-08 |
| Model Number | C8401 |
| Catalog Number | 101356101 |
| Lot Number | 1351094 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | APPLIED MEDICAL RESOURCES |
| Manufacturer Address | 22872 AVENIDA EMPRESA RANCHO SANTA MARGARITA CA 92688 US 92688 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-08 |