Demo stand-in. Nothing here reaches FDA.

eMDR receiver

Stands in for an electronic Medical Device Report submission route. POST a 3500A data set as XML or JSON to /submit; the answer is an acknowledgment number.

Received (1)

ESG-20261103-0001 (2026-11-03T03:33:59Z, xml, 1026 bytes)

Warnings: manufacturer report number

<?xml version="1.0" encoding="UTF-8"?><MedWatch3500A><ReportType>30-day</ReportType><ManufacturerReportNumber>3012345678-2026-84632</ManufacturerReportNumber><ComplaintNumber>CMP-284632</ComplaintNumber><CaseReference>NFQ-21</CaseReference><SectionB_Event><AdverseEventOrProductProblem>Product problem</AdverseEventOrProductProblem><DateOfEvent>2026-11-02</DateOfEvent><EventDescription/><PatientInvolvement>no-injury</PatientInvolvement></SectionB_Event><SectionD_Device><BrandName>Nexa Edge Vehicle</BrandName><Model>NXE-V</Model><UDI>(01)00860012340077(21)NXV-25-00631</UDI><Lot>25-207</Lot><SerialNumber>NXV-25-00631</SerialNumber><Firmware>5.2.0</Firmware><Manufacturer>Nexaform Labs, Minneapolis, MN</Manufacturer></SectionD_Device><SectionH_Manufacturer><DateManufacturerAware>2026-11-03</DateManufacturerAware><DeviceEvaluated>Pending return</DeviceEvaluated><ReportSource>User facility (Winterfield Health)</ReportSource><CorrectiveAction>Under investigation</CorrectiveAction></SectionH_Manufacturer></MedWatch3500A>