Access growing Medical Device Markets around the world with IECEE CB Scheme Testing and Certification from Intertek's four IECEE National Certification Bodies
The IECEE CB Scheme offers a one-stop approach to obtain multiple national safety certifications with a single CB Test Certificate and Report.
The IECEE Scheme, based on IEC and ISO harmonized international standards, allows for a true one-stop approach to obtain multiple national safety certifications with a single CB Test Certificate and Report. The program helps reduce trade barriers caused by different certification requirements in different countries, allowing Medical Device manufacturers to access existing, new and developing global markets. It eliminates delays and costs for repetitive testing, allowing companies to market their products faster while reducing overall costs.
Differences between the EU MDD and the MDR
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Countries Participating in the CB Scheme
- Argentina
- Australia
- Austria
- Bahrain
- Belarus
- Belgium
- Brazil
- Bulgaria
- Canada
- Chile
- China
- Columbia
- Croatia
- Czech Republic
- Côte d'Ivoire
- Denmark
- Finland
- France
- Germany
- Greece
- Hungary
- IndiaIndonesia
- Ireland
- Israel
- Italy
- Japan
- Kenya
- Republic of Korea
- Malaysia
- Mexico
- Netherlands
- New Zealand
- Nigeria
- Norway
- Pakistan
- Poland
- Portugal
- Russian Federation
- Saudi Arabia
- Serbia
- Singapore
- Slovakia
- Slovenia
- South Africa
- Spain
- Sweden
- Switzerland
- Thailand
- Turkey
- Ukraine
- United Arab Emirates
- United Kingdom
- United States of America
- Vietnam
Local Testing for Worldwide Safety Compliance
Through our global network of testing labs, Intertek possesses four National IECEE CB Scheme Certification Bodies (NCBs) in Singapore, Sweden, the United Kingdom and the United States of America for more than 45 associated CB Testing Laboratories worldwide.
Knowledge Center
Evolution of the Home Healthcare Market and Medical Device Compliance
White Paper | Webinar Recording
Ventilator Production: Introductory Guide to Regulatory Requirements
Critical Care Medical Devices: First-In-Queue Priority
Product Listing & Marking Strategies White Paper
IEC 60601-1-2 Edition 4 White Paper
Updated FCC Approval Process Webinar
Extractables and Leachables Studies Fact Sheet
Five Steps to Medical Device Commercialization in the United States White Paper
Making Green Profitable: Using IEC 60601-1-9 as a Competitive Advantage White Paper
Related Links
- ETL Mark The Industry's Fastest Certification Program
- Search and Buy Medical Device Standards
- Reese's Law – ANSI/UL 4200A-2023
- My Test Central
- Directories
- Certification Marks
- Global Research & Certification
- Medical Podcast - Compliance with Clarissa
- Satellite Data Acceptance Program
- Planning for Quality through Disruptions
- Intertek's world-class team of Medical Experts
- Intertek Protek - The world’s first industry-agnostic, end-to-end health, safety and wellbeing assurance program
*The Intertek legal entities that provide medical device management system certification services (including ISO 13485 and MDSAP) and Notified Body services (MDR 2017/745 and MDD 93/42/EEC) do not provide any consulting services. Clients who have used other Intertek legal entities’ consulting services are not eligible to receive management system certification services or Notified Body services from Intertek.
