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POST
/
api
/
v1
/
submit
/
EU_UDI_MDR
curl --request POST \
  --url https://api.udiconnect.io/api/v1/submit/EU_UDI_MDR \
  --header 'Authorization: <api-key>' \
  --header 'Content-Type: application/json' \
  --data '"{\n  \"actorCode\": \"DE-MF-000001723\",\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  \"agency\": \"EC\",\n  \"requestId\": \"string\",\n  \"modelInformation\": \"string\",\n  \"status\": \"SUCCESS\",\n  \"statusText\": \"Submission successfully validated and accepted\"\n}"

Authorizations

​
Authorization
string
header
required

Body

application/json

Data to be submitted

​
actorCode
string
​
securityToken
string
​
device
object

required for all EC submissions

​
deviceGroup
object

required for all EC submissions if not already submitted & published

Response

Submission processed successfully

Response for successful submission processing

​
agency
enum<string>

Regulatory agency information

Available options:
COMMON_DEVICE_DATA,
FDA,
EC,
NMPA,
MFDS,
GDSN,
SFDA,
TFDA,
TGA,
HSA
​
requestId
string

The unique identifier for the submission request

​
modelInformation
string

Information about the model and use case data used for processing the request

​
status
enum<string>

Submission response status

Available options:
INTERNAL_ERROR,
SUCCESS,
BLOCKED,
VALIDATION_FAILED
​
statusText
string

Description of the status