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RoHS 3.0 on Astek Power Supplies Unit4
Astek Globe 9Fl-1., No. 428, Chung Hsiao E. Road, Xizhi Dist., New Taipei City, Taiwan
UKCA(UK Conformity Assessed)   After the Brexit transition period ends, from January 1, 2021, there is a new safety approvals for switching power supplies and medical adapters/open frames in UK market, when importing to the UK market must comply with the requirements of UKCA (UK Conformity Assessed). UKCA covers most of the current EU CE regulations. The UK market includes England, Wales and Scotland, but excluding Northern Ireland. The UKCA mark is only applicable to the UK which cannot be applied to the European Union, European Economic Area or Northern Ireland market.   *UKCA requirements* Under the following conditions, the product shall be with “UKCA” logo from January 1, 2021. • Products sold in the UK • Products within the scope of British law • Must pass a third-party qualification assessment • Those who originally used the UK Notified Body and hasn’t transfer the conformity assessment file to the EU Notified Body before January 1, 2021 The above requirements don’t include the existing inventory entered the UK market before January 1, 2021, regardless of whether the verification is carried out by a UK institution.   UKCA, but starting from January 1, 2022, all products need to use the UKCA logo.   North Ireland products (unrestricted) CE or CE+UKNI   *UK Conformity Assessed, UKCA UK Conformity Assessment*   • UKCA (British Conformity Assessment) is a new British product conformity mark, used to show that the product complies with relevant British standards and regulatory requirements. • From January 1, 2021, products sold to the UK market (England, Wales and Scotland, but excluding Northern Ireland) must meet relevant UK standards and regulations before they can use the UKCA mark. The testing standards and verification process are basically the same as the current CE requirements. • The UKCA mark is only applicable to the UK and cannot be applied to the European Union, European Economic Area or Northern Ireland market.   Astek Power Supplies and Medical Adapter and Open Frames meet with UKCA approvals. For more information required, please contact info@astekglobe.com. https://www.astekglobe.com/hot_389550.html UKCA(UK Conformity Assessed) 2021-12-07 2022-12-07
Astek Globe 9Fl-1., No. 428, Chung Hsiao E. Road, Xizhi Dist., New Taipei City, Taiwan https://www.astekglobe.com/hot_389550.html
Astek Globe 9Fl-1., No. 428, Chung Hsiao E. Road, Xizhi Dist., New Taipei City, Taiwan https://www.astekglobe.com/hot_389550.html
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2021-12-07 http://schema.org/InStock $NT 0 https://www.astekglobe.com/hot_389550.html
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RoHS 3.0 (The Restriction of Hazardous Substances in Electrical and Electronic Equipment) on Astek Power Supplies Unit

Astek Switching Power Supplies are the compliance of RoHS 3.0.

In the world, many countries have their own RoHS directives. There are small differences among them. Mostly, they follow RoHS in Europe and America. Especially, CE includes RoHS and WEEE to lessen the shock from the wastes of Electrical and Electronic Equipment.

Switching Power Supplies are categorized into RoHS. In 2003, EU released RoHS 2002/95/EC, which is replaced by Directive 2011/68/EU on July 11 of 2011 and renewed the contents from Directive (EU) 2015/863 on June 4 of 2015. In 2018, RoHS 3 is announced and enforced on July 22 of 2019 for IT and consume electronics. Medical grade will be July 22 of 2021.

RoHS 3 expands the prohibited substances from six to ten by increasing new types of phthalates.

RoHS 6 prohibited substances:

Lead (Pb) <1000ppm

Cadmium (Cd)<100ppm

Mercury (Hg)<1000ppm

Hexavalent Chromium (Cr6+) <1000ppm

PBB <1000ppm

PBDE <1000ppm


New 4 phthalates add into RoHS 3:

Bis(2-ethylhexyl) Phthalate (DEHP) <1000ppm

Butyl benzyl phthalates (BBP)<1000ppm

Dibutyl phthalates (DBP) <1000ppm

Diisobutyl phthalates (DIBP) <1000ppm


For more information, please inquired us.

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