MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-28 for LOGOS 61502/140 manufactured by Milestone S.r.l..
Report Number | 1000391282-2019-00001 |
MDR Report Key | 8938652 |
Date Received | 2019-08-28 |
Date of Report | 2019-08-28 |
Date of Event | 2019-08-01 |
Date Mfgr Received | 2019-08-07 |
Device Manufacturer Date | 2015-03-20 |
Date Added to Maude | 2019-08-28 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. FRANCESCO VISINONI |
Manufacturer Street | VIA FATEBENEFRATELLI, 1/5 |
Manufacturer City | SORISOLE, BERGAMO 24010 |
Manufacturer Country | IT |
Manufacturer Postal | 24010 |
Manufacturer G1 | MILESTONE S.R.L. |
Manufacturer Street | VIA FATEBENEFRATELLI, 1/5 |
Manufacturer City | SORISOLE, 24010 |
Manufacturer Country | IT |
Manufacturer Postal Code | 24010 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | LOGOS |
Generic Name | AUTOMATED TISSUE PROCESSOR |
Product Code | IEO |
Date Received | 2019-08-28 |
Model Number | 61502/140 |
Catalog Number | 61502/140 |
Device Expiration Date | 2015-03-20 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 4 YR |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MILESTONE S.R.L. |
Manufacturer Address | VIA FATEBENEFRATELLI, 1/5 SORISOLE, 24010 IT 24010 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-28 |