FDA tightens entry rules for unregistered device makers. Learn how new FDA registration, U.S. Agent, and product listing checks may trigger detention and disrupt U.S.-bound medical device shipments.

ANVISA tightens filing rules for AI beauty devices in Brazil. Learn the new registration requirements, local clinical report needs, and how exporters can protect market access.

CPSC Alert adds a new UL 2849 test for wearables entering the U.S. from Oct 1, 2026. Learn the compliance impact, affected products, and what exporters and brands should do now.

Brazil Tightens AI Filing for Beauty Devices: learn how ANVISA’s 2026 rule impacts AI beauty device registration, clinical evidence, and Brazil market access before the deadline.

Brazil ANVISA requires AI filing for beauty devices from Q3 2026. Learn new Class III compliance rules, clinical evidence needs, and how to avoid registration delays.

Brazil Tightens AI Filing for Beauty Devices: learn how ANVISA’s new AI beauty device registration rules in Brazil could impact compliance, clinical documents, local licensing, and market entry plans.

EU Updates RoHS Annex II with four nano material limits, adding CNTs, nano-TiO2, nano-ZnO, and nano-Ag at ≤0.01% w/w. Learn the 2027 compliance impact on exporters and supply chains.

Brazil ANVISA Rule adds AI filing for beauty devices, requiring algorithm documents and validated clinical evidence. Learn how exporters can prepare faster for Brazil market access.