TīmeklisFetaLink+ GUDID 00853023006210 CERNER CORPORATION. FDA.report › GUDID › CERNER CORPORATION › 00853023006210. Obstetrics information system application software. Primary Device ID: 00853023006210: NIH Device Record Key: af892146-c28a-41dc-947e-3be19d4ebe43: Commercial Distribution Status: In … TīmeklisFetaLink+ transforms the ongoing measurements into a visual wave display which conveys the frequency, duration and relative strength of uterine contractions combined with the patient data of pregnant women in the antepartumn and/or intrapartum phases of pregnancy. Summary of the technological characteristics of the device compared …
FETALINK+ Trademark of CERNER INNOVATION, INC.. Serial …
Tīmeklis2012. gada 21. nov. · The FDA cleared Cerner‘s (Kansas CIty, MO) FetaLink+ mobile fetal monitoring app that provides clinicians the ability to check from anywhere maternal and fetal data of patients in the clinic. Tīmeklis2014. gada 7. janv. · Cerner Health Care Leaders - Cerner Corporation omm for constipation
Cerner Health Care Leaders - Cerner Corporation
TīmeklisFetaLink+® - FetaLink+4. Device Description. An application software program, routines, and/or algorithms used as or in an information system to electronically receive, collect, store, manage, assist in analysis of, display, output, and distribute data, within or between healthcare facilities, to support the administrative and clinical activities … TīmeklisWith FetaLink+, surveillance information that is available at the bedside can be accessed from any location through an iOS mobile device with... iOS. FetaLink+ … TīmeklisCERNER FETALINK+(VERSION1.0) System, Monitoring, Perinatal CERNER CORP. FDA.report › PMN › CERNER CORP. › K121758. The following data is part of a premarket notification filed by Cerner Corp. with the FDA for Cerner Fetalink+(version1.0). Pre-market Notification Details. Device ID: K121758: 510k … is army wives on hulu