27/08/2026
🚨 Medical Device Manufacturers — Are You Ready to Export?
Do you already have a medical device, factory, ISO 13485, CE, test reports, or technical documents — but you're stuck with registration or export requirements?
Don’t start from zero. Start from where you are.
We help medical device manufacturers identify what is missing and complete the regulatory & export pathway for markets such as:
🇬🇧 UK | 🇪🇺 EU | 🇪🇬 Egypt | 🇸🇦 Saudi Arabia | 🇦🇪 UAE | 🇨🇳 China | 🇮🇳 India | 🌍 International Markets
Our services include:
✅ ISO 13485 & Quality Management Systems
✅ CE / MDR Technical Documentation
✅ Medical Device Registration
✅ Free Sale Certificates
✅ Technical File Review & Gap Assessment
✅ Product & Manufacturer Documentation
✅ Export / Import Regulatory Requirements
✅ Regulatory Consulting & Market Entry Support
Already have documents? Great.
Send us what you have, and we will tell you what is missing, what needs to be corrected, and what the next step is.
📲 WhatsApp: 01140498546
Send “MEDICAL DEVICE” on WhatsApp for an initial assessment.
Alfa Pro Global Capital
Medical Device Regulatory & Certification Solutions