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Recent Posts
- Why Does EMC Testing of a Medical Device to IEC 60601-1-2, AIM 7351731, and/or Common EM Emitters Testing Have to be Conducted in Both Charging and Battery Modes? (Even When the Device Is Basically Just Napping on the Charger)
 - Is My Specially Designed Equipment in the Scope of RoHS?
 - Why ISO/IEC 17025 Accreditation Matters for Electrical Safety & EMC Testing | F2 Labs
 - We Offer CE Marking Training For Your Organization
 - So You Need to Field Evaluate Your Equipment – What You Need to Know
 
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Category Archives: Consulting
RoHS 2011/65/EU and Machinery
F2 Labs assists many manufacturers, internationally, with CE marking requirements. Regarding CE marking, primarily we test and evaluate electro-mechanical equipment for compliance with electrical safety, machinery safety, EMC and radio, medical device, and hazardous location requirements. However, when a manufacturer … Continue reading
									
						Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EMC Directive 2014/30/EU, General Product Safety Directive 2001/95/EC, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Regulation (EU)2017/745, Product Testing, Radio Equipment Directive 2014/53/EU, RoHS Directive 2011/65/EU					
					
				
								
					Tagged CE, CE mark, CE marking, EN 50581:2012, EU declaration of conformity, RoHS, RoHS 2, RoHS 2011/65/EU, RoHS compliance, WEEE, WEEE 2012/19/EU				
				
				
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		FCC – New Labeling and Manual Requirements
The FCC released new guidance and procedures for manufacturers to show compliance with FCC regulations in June 2017. Some of the changes are in the labeling requirements and, notably, the allowance for the use of a Suppliers Declaration of Conformity, or … Continue reading
									
						Posted in Consulting, FCC					
					
				
								
					Tagged EMC compliance, EMC testing, EMI testing, Emissions, FCC, FCC compliance, FCC ID, FCC Labeling, FCCID, Immunity, SDOC, Suppliers Declaration of Conformity				
				
				
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		EU’s Rapid Alert System for dangerous non-food products
The EU has a direct conduit for market surveillance authorities to communicate information about non-compliant products directly between 31 EU member nations and the European Commission. This system is called the Rapid Alert System, or RAPEX. This is not where … Continue reading
									
						Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EMC Directive 2014/30/EU, EN 60601-1, General Product Safety Directive 2001/95/EC, IP Testing, Lasers, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Regulation (EU)2017/745, PPE Regulation (EU) 2016/425, Pressure Equipment Directive 2014/68/EU, Product Testing, Radio Equipment Directive 2014/53/EU, RoHS Directive 2011/65/EU					
					
				
								
					Tagged CE, CE mark, CE marking, EU consumer protection, EU market surveillance, European Commission, European compliance, RAPEX, Rapid Alert System				
				
				
				Comments Off on EU’s Rapid Alert System for dangerous non-food products