MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,study report with the FDA on 2019-11-25 for NEXEL ELBOW ARTICULATION KIT SIZE N/A 00840009400 manufactured by Zimmer Biomet, Inc..
| Report Number | 0001822565-2019-04992 |
| MDR Report Key | 9368632 |
| Report Source | HEALTH PROFESSIONAL,STUDY |
| Date Received | 2019-11-25 |
| Date of Report | 2019-11-22 |
| Date of Event | 2015-11-10 |
| Date Mfgr Received | 2019-11-15 |
| Device Manufacturer Date | 2014-12-18 |
| Date Added to Maude | 2019-11-25 |
| 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. CHRISTINA ARNT |
| Manufacturer Street | 56 E. BELL DR. |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal | 46582 |
| Manufacturer Phone | 5745273773 |
| Manufacturer G1 | ZIMMER BIOMET, INC. |
| Manufacturer Street | 56 E. BELL DRIVE |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 46582 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NEXEL ELBOW ARTICULATION KIT SIZE |
| Generic Name | PROSTHESIS, ELBOW |
| Product Code | JDC |
| Date Received | 2019-11-25 |
| Model Number | N/A |
| Catalog Number | 00840009400 |
| Lot Number | 62875488 |
| Device Expiration Date | 2019-11-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ZIMMER BIOMET, INC. |
| Manufacturer Address | 56 E. BELL DRIVE WARSAW IN 46582 US 46582 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-11-25 |