MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-28 for PALINDROME 8888541044P manufactured by Covidien Mfg Solutions S.a..
Report Number | 3009211636-2020-00059 |
MDR Report Key | 9771262 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-02-28 |
Date of Report | 2020-03-27 |
Date of Event | 2020-02-07 |
Date Mfgr Received | 2020-03-10 |
Device Manufacturer Date | 2017-08-31 |
Date Added to Maude | 2020-02-28 |
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 | LISA HERNANDEZ |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | COVIDIEN MFG SOLUTIONS S.A. |
Manufacturer Street | EDIFICIO B20, CALLE #2 |
Manufacturer City | ALAJUELA 20101 |
Manufacturer Postal Code | 20101 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PALINDROME |
Generic Name | CATHETER, HEMODIALYSIS, IMPLANTED |
Product Code | MSD |
Date Received | 2020-02-28 |
Model Number | 8888541044P |
Catalog Number | 8888541044P |
Lot Number | 1723400100 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN MFG SOLUTIONS S.A. |
Manufacturer Address | EDIFICIO B20, CALLE #2 ALAJUELA 20101 20101 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-28 |