MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-02-14 for SURGIFLO HAEMOSTATIC MATRIX PRODUCT CODE MS0010 manufactured by Ferrosan Medical Devices A/s.
Report Number | 3008478369-2020-00002 |
MDR Report Key | 9710925 |
Report Source | DISTRIBUTOR |
Date Received | 2020-02-14 |
Date of Report | 2020-02-14 |
Date of Event | 2019-12-04 |
Date Mfgr Received | 2020-01-24 |
Device Manufacturer Date | 2019-05-29 |
Date Added to Maude | 2020-02-14 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | FERROSAN MEDICAL DEVICES A/S |
Manufacturer Street | SYDMARKEN 5 |
Manufacturer City | SOEBORG, 2860 |
Manufacturer Country | DA |
Manufacturer Postal | 2860 |
Manufacturer G1 | FERROSAN MEDICAL DEVICES A/S |
Manufacturer Street | SYDMARKEN 5 |
Manufacturer City | SOEBORG, 2860 |
Manufacturer Country | DA |
Manufacturer Postal Code | 2860 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SURGIFLO HAEMOSTATIC MATRIX PRODUCT CODE MS0010 |
Generic Name | SURGIFLO |
Product Code | LMF |
Date Received | 2020-02-14 |
Lot Number | 256823 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | FERROSAN MEDICAL DEVICES A/S |
Manufacturer Address | SYDMARKEN 5 SOEBORG, 2860 DA 2860 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-02-14 |