MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-25 for SPLINT, HAND AND COMPONENTS manufactured by Unk.
| Report Number | MW5088403 | 
| MDR Report Key | 8831329 | 
| Date Received | 2019-07-25 | 
| Date of Report | 2019-07-25 | 
| Date of Event | 2019-02-01 | 
| Date Added to Maude | 2019-07-26 | 
| Event Key | 0 | 
| Report Source Code | Voluntary report | 
| Manufacturer Link | N | 
| 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 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 0 | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 2 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 3 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 4 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 5 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Brand Name | SPLINT, HAND AND COMPONENTS | 
| Generic Name | SPLINT, HAND AND COMPONENTS | 
| Product Code | ILH | 
| Date Received | 2019-07-25 | 
| Device Availability | * | 
| Device Eval'ed by Mfgr | I | 
| Device Sequence No | 6 | 
| Device Event Key | 0 | 
| Manufacturer | UNK | 
| Manufacturer Address | UNK UNK | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-07-25 |