MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-11-29 for GH3 PATIENT LIFT manufactured by V. Guldmann A/s.
Report Number | 9391739 |
MDR Report Key | 9391739 |
Date Received | 2019-11-29 |
Date of Report | 2019-11-26 |
Date of Event | 2019-11-22 |
Report Date | 2019-11-26 |
Date Reported to FDA | 2019-11-26 |
Date Reported to Mfgr | 2019-11-29 |
Date Added to Maude | 2019-11-29 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
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 | 3 |
Brand Name | GH3 PATIENT LIFT |
Generic Name | LIFT, PATIENT, AC-POWERED |
Product Code | FSA |
Date Received | 2019-11-29 |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | V. GULDMANN A/S |
Manufacturer Address | 5525 JOHNS ROAD SUITE 905 TAMPA FL 33634 US 33634 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-29 |