MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-24 for OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 0500318E manufactured by Ogden Manufacturing Plant.
Report Number | 1713747-2020-00078 |
MDR Report Key | 9874177 |
Report Source | USER FACILITY |
Date Received | 2020-03-24 |
Date of Report | 2020-03-24 |
Date of Event | 2020-03-16 |
Date Mfgr Received | 2020-03-17 |
Device Manufacturer Date | 2019-11-10 |
Date Added to Maude | 2020-03-24 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MATTHEW AMARAL |
Manufacturer Street | 920 WINTER ST |
Manufacturer City | WALTHAM MA 02451 |
Manufacturer Country | US |
Manufacturer Postal | 02451 |
Manufacturer Phone | 7816999758 |
Manufacturer G1 | OGDEN MANUFACTURING PLANT |
Manufacturer Street | DIRECTOR, SITE QUALITY 475 WEST 13TH STREET |
Manufacturer City | OGDEN UT 84404 |
Manufacturer Country | US |
Manufacturer Postal Code | 84404 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OPTIFLUX 180NRE DIALYZER FINISHED ASSY. |
Generic Name | DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM |
Product Code | KDI |
Date Received | 2020-03-24 |
Model Number | 0500318E |
Catalog Number | 0500318E |
Lot Number | 19PU01004 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | MO |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | OGDEN MANUFACTURING PLANT |
Manufacturer Address | DIRECTOR, SITE QUALITY 475 WEST 13TH STREET OGDEN UT 84404 US 84404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-24 |