MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-02-21 for VACUETTE? TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 454322 manufactured by Greiner Bio-one Gmbh.
Report Number | 8020040-2016-00019 |
MDR Report Key | 9741944 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-02-21 |
Date of Report | 2020-02-21 |
Date Mfgr Received | 2015-11-22 |
Device Manufacturer Date | 2015-07-24 |
Date Added to Maude | 2020-02-21 |
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 | MANFRED ABEL |
Manufacturer Street | 4238 CAPITAL DRIVE |
Manufacturer City | MONROE NC 28110 |
Manufacturer Country | US |
Manufacturer Postal | 28110 |
Manufacturer Phone | 7042617800 |
Manufacturer G1 | GREINER BIO-ONE NA INC |
Manufacturer Street | 4238 CAPITAL DRIVE |
Manufacturer City | MONROE NC 28110 |
Manufacturer Country | US |
Manufacturer Postal Code | 28110 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VACUETTE? TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% |
Generic Name | TUBES, VACUUM SAMPLE, WITH ANTICOAGULANT |
Product Code | GIM |
Date Received | 2020-02-21 |
Model Number | 454322 |
Catalog Number | 454322 |
Lot Number | A15073SN |
Device Expiration Date | 2017-01-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GREINER BIO-ONE GMBH |
Manufacturer Address | BAD HALLER STR. 32 KREMSMUNSTER, AUSTRIA 4550 AU 4550 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-02-21 |