MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-31 for CAPIOX FX05 CX-FX05RE manufactured by Terumo Corporation, Ashitaka.
Report Number | 9681834-2020-00048 |
MDR Report Key | 9902732 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-12 |
Date Mfgr Received | 2020-03-12 |
Device Manufacturer Date | 2019-10-10 |
Date Added to Maude | 2020-03-31 |
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 Contact | THERESA MUSSAW |
Manufacturer Street | REG. NO. 2243441 265 DAVIDSON AVE SUITE 320 |
Manufacturer City | SOMERSET, NJ |
Manufacturer Country | US |
Manufacturer Phone | 2837866718 |
Manufacturer G1 | TERUMO CORPORATION, ASHITAKA |
Manufacturer Street | REG. NO. 9681834 150 MAIMAIGI-CHO |
Manufacturer City | FUJINOMIYA CITY, 418 |
Manufacturer Country | JA |
Manufacturer Postal Code | 418 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAPIOX FX05 |
Generic Name | OXYGENATOR, CARDIOPULMONARY BYPASS |
Product Code | DTZ |
Date Received | 2020-03-31 |
Returned To Mfg | 2020-03-14 |
Model Number | NA |
Catalog Number | CX-FX05RE |
Lot Number | 191010 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TERUMO CORPORATION, ASHITAKA |
Manufacturer Address | 150 MAIMAIGI-CHO FUJINOMIYA CITY, 418 JA 418 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other; 2. Required No Informationntervention | 2020-03-31 |