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Author Archives: F2 IT
Great Britain Changed the UKCA Deadline for Implementation, Again
The COVID-19 pandemic has thrown us all for a loop. Effects of the pandemic have been seen across many industries, supply chains, and more, including the extension of deadlines for product compliance regulations. In a statement on August 24th, 2021, … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, EN 60601-1, General Product Safety Regulation (EU) 2023/988, GPSR, GPSR (EU)2023/988, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Machinery Regulation (EU)2023/1230, Medical Devices Regulation (EU)2017/745, Pressure Equipment Directive 2014/68/EU, Product Testing, Radio Equipment Directive 2014/53/EU, REACH, RoHS Directive 2011/65/EU
Tagged UKCA
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F2 Labs’ is Officially Approved as an FDA ASCA-Accredited Testing Lab!
F2 Labs is officially an ASCA-accredited testing laboratory! We are one of only 17 labs approved by the FDA. This program will help increase product safety for the end-user and shorten the time it takes for FDA approval of your product. Continue reading
Posted in ASCA Program
Tagged accreditation, ASCA, compliance testing, FDA, safety testing
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The FDA’s ASCA Program and What it Means
This is the first time in history that the FDA has had a list of approved labs. F2 Labs is officially an ASCA-accredited testing laboratory. Continue reading
Posted in ASCA Program, FCC, FDA
Tagged ASCA, FDA, Medical Device, medical device testing
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What is the UKCA Marking?
The UK has left the EU and new rules concerning the transition for most CE products to UKCA products began in January 2021. The transition period for most products ends on December 31, 2021. All products shipped into the UK … Continue reading
Posted in UKCA
Tagged Brexit, UK conformity, UK Product Labeling, UK Technical Documentation, UKCA
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