MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-03-31 for LIBERTY SELECT CYCLER ASSY(NON-VALUATED) 180343 RTLR180343 manufactured by Concord Manufacturing.
Report Number | 2937457-2020-00565 |
MDR Report Key | 9905351 |
Report Source | COMPANY REPRESENTATIVE,CONSUM |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-19 |
Date Mfgr Received | 2020-03-19 |
Device Manufacturer Date | 2017-08-26 |
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 |
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 | CONCORD MANUFACTURING |
Manufacturer Street | DIRECTOR, QUALITY SYSTEMS 4040 NELSON AVENUE |
Manufacturer City | CONCORD CA 94520 |
Manufacturer Country | US |
Manufacturer Postal Code | 94520 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIBERTY SELECT CYCLER ASSY(NON-VALUATED) |
Generic Name | SYSTEM, PERITONEAL, AUTOMATIC DELIVERY |
Product Code | FKX |
Date Received | 2020-03-31 |
Model Number | 180343 |
Catalog Number | RTLR180343 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | MO |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONCORD MANUFACTURING |
Manufacturer Address | DIRECTOR, QUALITY SYSTEMS 4040 NELSON AVENUE CONCORD CA 94520 US 94520 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |