MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-17 for T.W. POWER SUPPLY VH-3010 manufactured by Maquet Cardiovascular Llc.
Report Number | 2242352-2020-00066 |
MDR Report Key | 9601433 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-01-17 |
Date of Report | 2020-02-07 |
Date of Event | 2019-12-31 |
Date Mfgr Received | 2020-02-06 |
Device Manufacturer Date | 2008-12-01 |
Date Added to Maude | 2020-01-17 |
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 Street | 45 BARBOUR POND DRIVE |
Manufacturer City | WAYNE NJ 07470 |
Manufacturer Country | US |
Manufacturer Postal | 07470 |
Manufacturer G1 | MAQUET CARDIOVASCULAR LLC |
Manufacturer Street | 45 BARBOUR POND DRIVE |
Manufacturer City | WAYNE NJ 07470 |
Manufacturer Country | US |
Manufacturer Postal Code | 07470 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | T.W. POWER SUPPLY |
Generic Name | UNIT, CAUTERY, THERMAL, AC-POWERED |
Product Code | HQO |
Date Received | 2020-01-17 |
Returned To Mfg | 2020-01-13 |
Model Number | T.W. POWER SUPPLY |
Catalog Number | VH-3010 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MAQUET CARDIOVASCULAR LLC |
Manufacturer Address | 45 BARBOUR POND DRIVE WAYNE NJ 07470 US 07470 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-17 |