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Certifications & Quality Assurance

ANTONMOVE is committed to global compliance and medical-grade safety standards. Our products are distributed under strict corporate governance and manufactured in partnership with certified medical device facilities.

Hong Kong Corporate Registration
Corporate Entity
Hong Kong Business Registration
Global Operations
Class III Medical Device Distribution License
Supply Chain Compliance
Class III Medical Device Sales License
High-Grade Medical
ISO 13485 Quality Management System
ISO 13485 Certified
Medical Devices Quality Management
Facility Audit
CE Mark Product Compliance
CE Certified
European Health & Safety Standards
EU Compliant
FDA Facility Registration
FDA Registered
US Medical Device Listing & Establishment
US Compliant
Supply Chain & Compliance Transparency: ANTONMOVE brand operations are managed by our registered entity in Hong Kong, with domestic supply chain management supported by our Class III Medical Device licensed operation in China. All medical consumables (including sterile needles, cannula, and PDO threads) are manufactured in strict compliance with ISO 13485, CE, and FDA standards by our contract manufacturing partners.