MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-04-05 for RESEARCH CRYOSTAT LEICA CM3050 S CM3050S 14047033510 manufactured by Leica Biosystems Nussloch Gmbh.
| Report Number | 1423337-2010-00003 |
| MDR Report Key | 1664964 |
| Date Received | 2010-04-05 |
| Date of Report | 2010-03-04 |
| Date of Event | 2010-02-22 |
| Date Facility Aware | 2010-03-04 |
| Report Date | 2010-04-02 |
| Date Reported to FDA | 2010-04-02 |
| Date Reported to Mfgr | 2010-03-04 |
| Date Added to Maude | 2010-04-22 |
| Event Key | 0 |
| Report Source Code | Distributor 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 | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RESEARCH CRYOSTAT LEICA CM3050 S |
| Generic Name | CRYOSTAT |
| Product Code | IDP |
| Date Received | 2010-04-05 |
| Model Number | CM3050S |
| Catalog Number | 14047033510 |
| Lot Number | NA |
| ID Number | NA |
| Operator | OTHER |
| Device Availability | Y |
| Device Age | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | LEICA BIOSYSTEMS NUSSLOCH GMBH |
| Manufacturer Address | HEIDELBERGER STR. 17-19 NUSSLOCH 6922 GM 6922 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2010-04-05 |