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 2020-03-12 for FINGER CUFF CSCM manufactured by Edwards Lifesciences Dr.
Report Number | 2015691-2020-10936 |
MDR Report Key | 9826030 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-12 |
Date of Report | 2020-02-24 |
Date of Event | 2020-02-24 |
Date Mfgr Received | 2020-02-24 |
Date Added to Maude | 2020-03-12 |
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 | MRS. SAMANTHA EVELEIGH |
Manufacturer Street | 1 EDWARDS WAY |
Manufacturer City | IRVINE CA 92614 |
Manufacturer Country | US |
Manufacturer Postal | 92614 |
Manufacturer Phone | 9492503939 |
Manufacturer G1 | EDWARDS LIFESCIENCES DR |
Manufacturer Street | PARQUE INDUSTRIAL DE ITABO CARR. SANCHEZ KM 18.5 |
Manufacturer City | HAINA, SAN CRISTOBAL |
Manufacturer Country | DR |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FINGER CUFF |
Generic Name | SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE |
Product Code | DXN |
Date Received | 2020-03-12 |
Model Number | CSCM |
Catalog Number | CSCM |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EDWARDS LIFESCIENCES DR |
Manufacturer Address | PARQUE INDUSTRIAL DE ITABO CARR. SANCHEZ KM 18.5 HAINA, SAN CRISTOBAL DR |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-12 |