{"@context":{"@vocab":"https://schema.org/","dcterms":"http://purl.org/dc/terms/"},"@type":"Organization","@id":"https://api.morvs.ai/medical-device-mfr/3017618900#org","identifier":[{"@type":"PropertyValue","propertyID":"FDA Establishment Identifier (FEI)","value":"3017618900"},{"@type":"PropertyValue","propertyID":"FDA Owner/Operator Number","value":"10078391"}],"name":"HUIZHOU GOLD ROSE TECHNOLOGY CO.,LTD","legalName":"HUIZHOU GOLD ROSE TECHNOLOGY CO.,LTD","parentOrganization":{"@type":"Organization","name":"Huizhou Gold Rose Technology Co.,Ltd","identifier":"10078391"},"address":{"@type":"PostalAddress","streetAddress":"LEFT 2ND FLOOR, NO.3 LEJIN NORTH ROAD, NO.24 DISTRICT, ZHONGKAI DEVELOPMENT ZONE","addressLocality":"huizhou Guangdong","addressRegion":null,"postalCode":"516000","addressCountry":"CN"},"additionalType":["Develop Specifications But Do Not Manufacture At This Facility","Export Device to the United States But Perform No Other Operation on Device","Foreign Private Label Distributor","Manufacture Medical Device for Another Party (Contract Manufacturer)","Repack or Relabel Medical Device","Complaint File Establishment per 21 CFR 820.198"],"additionalProperty":[{"@type":"PropertyValue","propertyID":"FDA Product Codes","value":"KMY"},{"@type":"PropertyValue","propertyID":"Registration expiry year","value":"2026"}],"sameAs":["https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3017618900"],"isAccessibleForFree":true,"license":"https://creativecommons.org/publicdomain/zero/1.0/","_source":{"data_provider":"AI Analytics","brand_name":"MORVS","brand_url":"https://morvs.ai/","data_provider_url":"https://api.morvs.ai","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://open.fda.gov/apis/device/registrationlisting/","generated_at":"2026-11-02T00:20:17.400Z"}}