Global Medical Device Registration, Testing & Compliance Services
EVERBIZ is a professional compliance service platform dedicated to medical device testing, certification, consulting and training. With offices in Shanghai (China), Hong Kong, Munich (Germany), Salzburg (Austria), Thailand, Malaysia, Singapore and Vietnam, we help medical device companies worldwide strengthen their regulatory compliance and accelerate their entry into international markets.
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Our Services
Registration, testing and regulatory consulting – a one-stop solution for taking your medical devices global
Medical Product Registration
As a company registered with the German medical device authority, EVERBIZ GmbH provides professional registration services for medical products and devices in multiple countries, opening the door to markets around the world.
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Product Testing
EVERBIZ GmbH has experienced product testing specialists who provide a full range of testing and remediation consulting services, helping clients bring their products to Europe and the global market.
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Global Medical Device Registration Services
Our authorized representative and registration services cover the following countries and regions
Testing & Validation
Testing and validation services for medical devices and related products
Why Choose Us as Your Partner
Outstanding Multi-Country Service
EVERBIZ GmbH specializes in acting as a professional authorized representative in multiple countries, supporting clients with notifications, registrations and all follow-up communication, and providing expert advice and response strategies for every situation. We deliver end-to-end solutions that help clients bring their products smoothly to the global market.
Customer-Driven Approach
We design the optimal solution for each client’s product type, product characteristics and specific needs, paving the way to the European market with quality and efficiency.
A Professional, Reliable Team
EVERBIZ GmbH has a professional team whose members bring many years of technical experience in testing and certification. We know the relevant EU regulations and response strategies inside out, and offer Chinese, English and German language support with fast, efficient communication and feedback.
Strategic Location
Our company is based in Munich, the capital of Bavaria and the political, economic, cultural and research hub of southern Germany. Being close to the authorities allows us to respond quickly to any situation. Munich also borders southern European countries and offers excellent transport links, so communication runs smoothly even if you register your products in other European countries.
Latest Regulatory Updates
Medical device regulatory updates and registration guides
- 45 Days to Go: EUDAMED Registration of Existing Devices Closes on 28 November – Is Your Product Registered?
- China Issues New Medical Device GMP Inspection Guidelines: 200 Items in Three Risk Levels from 1 November
- [Sharing] A Medical Device Warehouse in Cleveland, USA, Open for Shared Use
- 5 Days to Go: Indonesia Halal Certification Mandatory for Class A Medical Devices from 18 October – Get the Three Dates Right
- New HSA Rule in Singapore: Incomplete Registration Applications Will Be Rejected from 2027
- How to Complete a CPNP Notification Before Placing Cosmetics on the EU Market
- Thailand Cracks Down on Non-Compliant Medical Devices: Registering Colored and Contact Lenses in Thailand
- The Updated EU Classification Guidance Explained: What Manufacturers Should Look at and Do
- A Must for ASEAN Market Entry: The Medical Device CSDT Submission Template Explained
- Singapore Medical Device Regulations Updated Again: Key HSA Changes in 2026 and How Companies Should Respond
Need a medical device registration or testing plan?
Tell us about your product and target markets, and we will provide professional compliance advice.
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