MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2020-03-09 for CONNECTA PLUS1 360 WHITE BLEND 394910 manufactured by Bd Infusion Therapy Systems Inc. S.a. De C.v..
Report Number | 9610847-2020-00088 |
MDR Report Key | 9808102 |
Report Source | DISTRIBUTOR,FOREIGN,OTHER |
Date Received | 2020-03-09 |
Date of Report | 2020-03-12 |
Date of Event | 2020-02-17 |
Date Mfgr Received | 2020-02-17 |
Device Manufacturer Date | 2018-01-19 |
Date Added to Maude | 2020-03-09 |
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 | BDX BRETT WILKO |
Manufacturer Street | 9450 SOUTH STATE STREET |
Manufacturer City | SANDY UT 84070 |
Manufacturer Country | US |
Manufacturer Postal | 84070 |
Manufacturer Phone | 8015652341 |
Manufacturer G1 | BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Street | PERIFERICO LUIS DONALDO COLOSIO NO. 579 |
Manufacturer City | NOGALES |
Manufacturer Country | MX |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CONNECTA PLUS1 360 WHITE BLEND |
Generic Name | STOPCOCK |
Product Code | FMG |
Date Received | 2020-03-09 |
Catalog Number | 394910 |
Lot Number | 8003803 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Address | PERIFERICO LUIS DONALDO COLOSIO NO. 579 NOGALES MX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-09 |