ISO 13485:2016 CE Marked FDA Establishment Registration EU MDR / IVDR Ready

A Trusted OEM/ODM Partner for Global Healthcare Brands Since 2005

Headquartered in Wenzhou, China, we work with ISO 13485:2016-certified partner facilities across 100,000+ sqm of automated workshops — an extension of your sourcing and documentation team.

2005
Founded in Wenzhou
100,000+ sqm
Automated Workshops
3
Product Divisions
5-Step
QC Inspection

Who We Are

A professional medical foreign trade enterprise with 20+ years of global supply-chain expertise.

Established in 2005 and headquartered in Lucheng District, Wenzhou, Zhejiang, China Med Supply is a professional medical foreign trade enterprise specializing in OEM/ODM solutions for medical devices, healthcare consumables, and aging-friendly products. Over the past two decades, we have grown from a regional trading company into a global supply-chain partner serving clients across Europe, North America, Oceania, and the Middle East.

Unlike scattered brokers who simply resell goods, we operate as an OEM supplier of medical devices, mobility aids and home healthcare supplies with ISO 13485-certified partner facilities, serving global brands since 2005, covering over 100,000 square meters of automated production workshops. Our role is to act as an extension of your sourcing and compliance team — aligning product development, quality control, and regulatory documentation with the specific requirements of your target market.

Our Story — Milestone Timeline

Over 20 years of growth, innovation, and global expansion.

  1. Company founded in Wenzhou, Zhejiang, starting as a domestic medical supplies trader.

  2. Expanded into international export, establishing first overseas client relationships in Europe.

  3. Achieved ISO 13485 certification; launched dedicated OEM/ODM service division.

  4. Partner factory network expanded to 100,000+ sqm automated production capacity.

  5. Full transition to EU MDR (2017/745) compliant processes; FDA registration support launched.

  6. Launched dedicated Mobility & Daily Living Aids line; expanded to Middle East and Latin American markets.

    Explore the Line
  7. Expanded digital supply-chain capabilities and upgraded quality control systems across partner facilities.

  8. Continuing to deepen digital and quality infrastructure — and welcoming next-generation global healthcare partners.

    Partner With Us

How We Work — Your Extension in China

From regulatory alignment to final delivery, we operate as a seamless extension of your sourcing and documentation team.

Integrated Sourcing & Documentation

We don't just resell products. Every SKU is reviewed against your target market's requirements before production begins.

SKU-Level Alignment

End-to-End Quality Oversight

From material selection and supplier qualification to batch traceability, we manage the full quality process — not just spot inspections.

Full Chain Control

Transparent Project Management

You get one dedicated account manager, real-time production updates, and zero black-box manufacturing.

One-on-One Service

Market-Adaptive Supply Solutions

Whether you need low-MOQ pilot batches or high-volume automated production, our supply model adapts to your business stage.

Scalable & Flexible

Quality & Compliance — Non-Negotiable Standards

In the medical and senior care industries, compliance is not optional — it is foundational.

ISO 13485:2016Quality management system maintained across our partner facilities
CE MarkingUnder EU MDR 2017/745, or EU IVDR 2017/746 for IVD products
FDA Establishment RegistrationRegistration held by our manufacturing sites
5-Step QC InspectionStandard applied to all sourced products
Material SelectionWhere applicable, materials selected for biocompatibility and latex-free requirements
Documentation SupportTechnical documentation, clinical or performance evaluation reports and Declarations of Conformity
Batch TraceabilityTraceability and stability testing for all production runs

Serving Global Markets with Local Market Knowledge

Whether you are launching a private-label line in Germany, expanding a distribution brand in the United States, or introducing senior care products to the Middle East — our team supports your market entry with documentation and supply solutions adapted to your region's requirements and business culture.

Europe

CE marking under EU MDR 2017/745 — or EU IVDR 2017/746 for IVD products — with technical documentation prepared to support your market entry.

EU MDR / IVDR

North America

Manufacturing sites hold FDA Establishment Registration, with quality systems aligned to FDA requirements; Canadian projects supported with Health Canada documentation.

FDA / Health Canada

Australia

TGA dossier preparation and ARTG listing support, with localized labeling for the Australian market.

TGA / ARTG

China

NMPA registration pathway support and cross-border e-commerce supply solutions.

NMPA

Middle East & Latin America

SFDA, MOH and ANVISA documentation support, with Arabic and Portuguese paperwork available.

SFDA / ANVISA

Your Market

Tell us your target country — we will outline the documentation typically required for your product.

Custom Pathway

Mission, Vision & Values

The principles that guide every decision we make.

Our Mission

To make safe, reliable healthcare and aging-friendly products accessible worldwide through responsible manufacturing and trusted partnerships.

We work with ISO 13485:2016-certified partner facilities and support every project with the documentation your market requires.

Our Vision

To become the preferred OEM partner for medical and senior care brands seeking well-documented, scalable and future-ready supply chain solutions from China.

Our Values

  • Requirements Alignment — your market requirements as baseline
  • Quality Without Compromise — checks at every stage
  • Transparent Partnership — clear pricing, open updates
  • Customer-Centric Innovation — built around your growth

Ready to Discuss Your Product Needs?

Get in touch for a free sample, custom quotation, or private-label proposal — we usually reply within 24 hours.

Request a Free Sample