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 2019-10-28 for 150 FASTURN SYRINGE KIT W/QFT 85232924 ART 700 SYR manufactured by Bayer Medical Care Inc..
Report Number | 2520313-2019-00049 |
MDR Report Key | 9245099 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-28 |
Date of Report | 2019-11-21 |
Date of Event | 2019-10-02 |
Date Mfgr Received | 2019-10-31 |
Device Manufacturer Date | 2018-09-05 |
Date Added to Maude | 2019-10-28 |
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 | DIANE ECKERT |
Manufacturer Street | 1 BAYER DRIVE |
Manufacturer City | INDIANOLA PA 15051 |
Manufacturer Country | US |
Manufacturer Postal | 15051 |
Manufacturer Phone | 7249408677 |
Manufacturer G1 | BAYER MEDICAL CARE INC. |
Manufacturer Street | 1 BAYER DRIVE |
Manufacturer City | INDIANOLA PA 15051 |
Manufacturer Country | US |
Manufacturer Postal Code | 15051 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 150 FASTURN SYRINGE KIT W/QFT |
Generic Name | ANGIOGRAPHIC SYRINGE KIT |
Product Code | DXT |
Date Received | 2019-10-28 |
Returned To Mfg | 2019-10-31 |
Model Number | 85232924 |
Catalog Number | ART 700 SYR |
Lot Number | 8409190 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAYER MEDICAL CARE INC. |
Manufacturer Address | 1 BAYER DRIVE INDIANOLA PA 15051 US 15051 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-28 |