D:î˜ Configure the MUSE System for Network Communication...................... 312
MUSEAPI3 Installation.................................................................................................................................... 312
Before You Start....................................................................................................................................312
Install MUSEAPI3 on MUSE v8 Server.........................................................................................313
Install MUSEAPI3 on MUSE v9 Server.........................................................................................319
Change the MUSEAPI3 Service Protocol Configuration..................................................... 323
Uninstall MUSEAPI3............................................................................................................................. 324
Restore the MUSEAPI3 Configuration.........................................................................................325
MUSEAPI Test Client............................................................................................................................ 325
Obtain the Thumbprint of the SSL Certificate for the MUSEAPI3 Port......................... 326
Set Up DCP Inbound Communication for MUSE v8.x or v9.x.......................................................328
Add the DCP Service and DCP Communication Option to the MUSE System...........328
Set Up the DCP Server Configuration in the MUSE System..............................................329
E:î˜ Configure the CardioSoft System for Network Communication..............331
CardioSoft V7 Installation.............................................................................................................................331
Set Up DCP Port in CardioSoft V7.0.........................................................................................................331
F:î˜ System Checkout..............................................................................................332
DCP Transmission to the MUSE System................................................................................................332
DCP Transmission to the CardioSoft System...................................................................................... 332
MUSE Order Download.................................................................................................................................. 332
G:î˜ Technical Specifications................................................................................. 333
System Specifications.....................................................................................................................................333
ECG Specifications............................................................................................................................................335
Environmental Specifications......................................................................................................................336
Safety Specifications.......................................................................................................................................337
Network Specifications.................................................................................................................................. 338
H:î˜ Regulatory and Safety Information............................................................. 339
Intended Use.......................................................................................................................................................339
Indications for Use...........................................................................................................................................339
Contraindications..............................................................................................................................................340
Clinical Benefits..................................................................................................................................................340
Prescription Device Statement...................................................................................................................340
Safety Conventions..........................................................................................................................................340
Safety Hazards...................................................................................................................................................341
Classification of Medical Device................................................................................................................344
Certification Information...............................................................................................................................345
Recording ECGs during Defibrillation......................................................................................................345
Modulating Effects in Digital Systems....................................................................................................346
Electromagnetic Compatibility (EMC)...................................................................................................... 346
Guidance and Manufacturer’s Declaration—Electromagnetic Emissions................. 347
Guidance and Manufacturer’s Declaration—Electromagnetic Immunity..................347
Essential Performance....................................................................................................................... 348
Biocompatibility................................................................................................................................................. 349
Legal Notice.........................................................................................................................................................349
Supplies and Accessories............................................................................................................................. 350
Responsibility of the Manufacturer..........................................................................................................350
Responsibility of the Purchaser/Customer...........................................................................................350
Notification to Member States...................................................................................................................350
Warranty Information.....................................................................................................................................350