MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-06 for SITUATE G0404-32P01C-1 manufactured by Mitg - Rf Surgical Systems.
Report Number | 3005883396-2020-00017 |
MDR Report Key | 9799958 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-03-06 |
Date of Report | 2020-03-22 |
Date of Event | 2020-02-19 |
Date Mfgr Received | 2020-02-28 |
Date Added to Maude | 2020-03-06 |
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 | LISA HERNANDEZ |
Manufacturer Street | 5920 LONGBOW DRIVE |
Manufacturer City | BOULDER CO 80301 |
Manufacturer Country | US |
Manufacturer Postal | 80301 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | MITG - RF SURGICAL SYSTEMS |
Manufacturer Street | 2101 FARADAY |
Manufacturer City | CARLSBAD CA 92008 |
Manufacturer Country | US |
Manufacturer Postal Code | 92008 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SITUATE |
Generic Name | GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE |
Product Code | GDY |
Date Received | 2020-03-06 |
Model Number | G0404-32P01C-1 |
Catalog Number | G0404-32P01C-1 |
Lot Number | 191009AF |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MITG - RF SURGICAL SYSTEMS |
Manufacturer Address | 2101 FARADAY CARLSBAD CA 92008 US 92008 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-06 |