China MedTech Export Radar

What it does

Recent China medical-device activity, turned into evidence-backed sales leads for FDA U.S. Agents, EU Authorised Representatives, UK Responsible Persons, and MedTech regulatory consultancies. Every lead includes a published business email, official website, registration references, confidence grades, and source links. Start with 5 companies at USD 49 or 10 at USD 99; free 3-company sample at med.97rg.com.

Recent China medical-device activity, turned into evidence-backed sales leads for U.S. Agents, EU/UK representatives, and MedTech regulatory consultancies. Start with 10 companies at USD 49 or the full current release at USD 99.

For U.S. Agents, EU/UK representatives, and MedTech regulatory consultancies. Test the evidence with a 10-company Starter or the full current release matched to your service. Chinese manufacturers filing new NMPA device records are your fastest-growing prospect pool. Each record shows the registrant, product category, and when the activity happened. EUDAMED Actor registration became mandatory in May 2026. Manufacturers with fresh domestic activity and export-ready signals are timely outreach targets for EU AR, UKRP, ISO 13485, and CE services. Source NMPA UDI daily releases (udid.nmpa.gov.cn), checksum-verified before parsing. Honest limits Recent NMPA activity is a commercial timing…from med.97rg.com

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