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 2020-02-13 for TUBING, PUMP, CARDIOPULMONARY BYPASS VKMO 71000 70106.7949 manufactured by Maquet Cardiopulmonary Gmbh.
Report Number | 8010762-2020-00057 |
MDR Report Key | 9705287 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-13 |
Date of Report | 2020-03-30 |
Date of Event | 2020-01-28 |
Date Mfgr Received | 2020-03-30 |
Device Manufacturer Date | 2019-07-08 |
Date Added to Maude | 2020-02-13 |
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 Street | MAQUET CARDIOPULMONARY AG KEHLER STRASSE 31 |
Manufacturer City | RASTATT 76437 |
Manufacturer Country | GM |
Manufacturer Postal | 76437 |
Manufacturer Phone | 4972229321 |
Manufacturer G1 | NURSEL BOELENS |
Manufacturer Street | MAQUET CARDIOPULMONARY AG KEHLER STRASSE 31 |
Manufacturer City | RASTATT 76437 |
Manufacturer Country | GM |
Manufacturer Postal Code | 76437 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TUBING, PUMP, CARDIOPULMONARY BYPASS |
Generic Name | TUBING, PUMP, CARDIOPULMONARY BYPASS |
Product Code | DWE |
Date Received | 2020-02-13 |
Returned To Mfg | 2020-03-02 |
Model Number | VKMO 71000 |
Catalog Number | 70106.7949 |
Lot Number | 92284996 |
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 CARDIOPULMONARY GMBH |
Manufacturer Address | NEUE ROTTENBURGER STRASSE 37 HECHINGEN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-13 |