IEC 61326-2-6 EMC Compliance Testing for IVD Medical Equipment
IEC 61326-2-6 specifies EMC requirements for in vitro diagnostic (IVD) medical equipment. Compatible Electronics provides comprehensive EMC testing for IVD devices to ensure electromagnetic compatibility and regulatory compliance.
Overview
IEC 61326-2-6 is the particular EMC standard for in vitro diagnostic medical equipment, supplementing IEC 61326-1 general requirements. It addresses the specific electromagnetic environment and performance criteria for IVD devices used in clinical laboratories.
Testing Services
Comprehensive Testing
Complete evaluation of your medical devices to ensure regulatory compliance and patient safety.
Expert Analysis
Our experienced engineers provide detailed technical analysis and documentation for your regulatory submissions.
Regulatory Support
Support for FDA 510(k), CE marking, and other global regulatory requirements.
Quick Turnaround
Efficient testing processes to meet your development timelines and market launch goals.
Standards We Test To
International
- IEC 61326-2-6 Ed. 2.0
- IEC 61326-2-6 Ed. 3.0
- IEC 61326-1 (general EMC)
European
- EN 61326-2-6 (European harmonized)
- CISPR 11 emission limits
- IEC 61000 series immunity
North America
- NVLAP accredited testing
- FDA recognized EMC standards
- US market compliance
Related Standards
- IEC 61010-2-101 (IVD safety)
- ISO 14971 (EMC risk management)
- IEC 61000 series (basic EMC)
Get Started Today
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