curl --request POST \
--url https://api.udiconnect.io/api/v1/validate/EU_UDI_MDR \
--header 'Authorization: <api-key>' \
--header 'Content-Type: application/json' \
--data '
"{\n \"device\": {\n \"IssuingAgency\": \"GS1\",\n \"Device\": \"00308676965723\",\n \"DeviceGroup\": \"439990237188JM\",\n \"Material\": \"37588-474\",\n \"BaseQuantity\": 1,\n \"CommercialDistributionStatus\": \"ON_THE_MARKET\",\n \"ProductionIdentifier\": [\n \"BATCH_NUMBER\"\n ],\n \"ReferenceNumber\": \"37588-474\",\n \"MDN\": [\n \"A0101010201\"\n ],\n \"NumberOfReuses\": 0,\n \"ContainsLatex\": false,\n \"Reprocessed\": false,\n \"Sterile\": false,\n \"ReqSterilizatonPriorUse\": true,\n \"MarketInfos\": [\n {\n \"Country\": \"DE\",\n \"OriginalPlacedOnTheMarket\": true\n }\n ],\n \"AdditionalTradeNames\": [\n {\n \"AdditionalTradeName\": \"Trade Name\",\n \"AdditionalTradeNameLanguage\": \"EN\"\n }\n ]\n },\n \"deviceGroup\": {\n \"DeviceGroupAgency\": \"GS1\",\n \"DeviceGroup\": \"439990237188JM\",\n \"ApplicableLegislation\": \"MDR\",\n \"MFActorCode\": \"DE-MF-000001723\",\n \"DeviceName\": \"Device Name\",\n \"RiskClass\": \"CLASS_I\",\n \"AnimalTissuesCells\": false,\n \"HumanTissuesCells\": false,\n \"DeviceImplantable\": false,\n \"DeviceHasMeasuringFunction\": false,\n \"DeviceReusableSurgicalInstrument\": false,\n \"ActiveDevice\": false,\n \"DeviceIntendedToAdministerMedicine\": false,\n \"SystemDevice\": false,\n \"ProcedurePackDevice\": false,\n \"HumanProductCheck\": false,\n \"MedicinalProductCheck\": false\n }\n}\n"
'"{\n \"status\": \"successful\",\n \"message\": \"Validation successful\"\n}"
API Documentation
EUDAMED MDR Validate
Validates UDI device data against the specified data model schema and business rules. This endpoint performs comprehensive validation including schema validation, business rule checks, and data integrity verification without actually submitting the data to regulatory agencies.
POST
/
api
/
v1
/
validate
/
EU_UDI_MDR
curl --request POST \
--url https://api.udiconnect.io/api/v1/validate/EU_UDI_MDR \
--header 'Authorization: <api-key>' \
--header 'Content-Type: application/json' \
--data '
"{\n \"device\": {\n \"IssuingAgency\": \"GS1\",\n \"Device\": \"00308676965723\",\n \"DeviceGroup\": \"439990237188JM\",\n \"Material\": \"37588-474\",\n \"BaseQuantity\": 1,\n \"CommercialDistributionStatus\": \"ON_THE_MARKET\",\n \"ProductionIdentifier\": [\n \"BATCH_NUMBER\"\n ],\n \"ReferenceNumber\": \"37588-474\",\n \"MDN\": [\n \"A0101010201\"\n ],\n \"NumberOfReuses\": 0,\n \"ContainsLatex\": false,\n \"Reprocessed\": false,\n \"Sterile\": false,\n \"ReqSterilizatonPriorUse\": true,\n \"MarketInfos\": [\n {\n \"Country\": \"DE\",\n \"OriginalPlacedOnTheMarket\": true\n }\n ],\n \"AdditionalTradeNames\": [\n {\n \"AdditionalTradeName\": \"Trade Name\",\n \"AdditionalTradeNameLanguage\": \"EN\"\n }\n ]\n },\n \"deviceGroup\": {\n \"DeviceGroupAgency\": \"GS1\",\n \"DeviceGroup\": \"439990237188JM\",\n \"ApplicableLegislation\": \"MDR\",\n \"MFActorCode\": \"DE-MF-000001723\",\n \"DeviceName\": \"Device Name\",\n \"RiskClass\": \"CLASS_I\",\n \"AnimalTissuesCells\": false,\n \"HumanTissuesCells\": false,\n \"DeviceImplantable\": false,\n \"DeviceHasMeasuringFunction\": false,\n \"DeviceReusableSurgicalInstrument\": false,\n \"ActiveDevice\": false,\n \"DeviceIntendedToAdministerMedicine\": false,\n \"SystemDevice\": false,\n \"ProcedurePackDevice\": false,\n \"HumanProductCheck\": false,\n \"MedicinalProductCheck\": false\n }\n}\n"
'"{\n \"status\": \"successful\",\n \"message\": \"Validation successful\"\n}"
Authorizations
Body
application/json
Data to be validated