MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-02-12 for NEOTECH PRODUCTS UNKNOWN manufactured by Neotech Products Llc.
| Report Number | 2025917-2020-00001 |
| MDR Report Key | 9702394 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2020-02-12 |
| Date of Report | 2020-02-12 |
| Date of Event | 2019-12-31 |
| Date Mfgr Received | 2020-01-14 |
| Date Added to Maude | 2020-02-12 |
| 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 | BEN MAHAJAN |
| Manufacturer Street | 28430 WITHERSPOON PARKWAY |
| Manufacturer City | VALENCIA, CA |
| Manufacturer Country | US |
| Manufacturer Phone | 7757466147 |
| Manufacturer G1 | NEOTECH PRODUCTS LLC |
| Manufacturer Street | 28430 WITHERSPOON PARKWAY |
| Manufacturer City | VALENCIA, CA |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NEOTECH PRODUCTS |
| Generic Name | NEOBAR |
| Product Code | CBH |
| Date Received | 2020-02-12 |
| Model Number | UNKNOWN |
| Catalog Number | UNKNOWN |
| Lot Number | N/A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | NEOTECH PRODUCTS LLC |
| Manufacturer Address | 28430 WITHERSPOON PARKWAY VALENCIA, CA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-12 |