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What is REACH detection? REACH detection notification

Date:2023-01-10 09:54:16 Classification :【question】 Visits:
What is REACH detection? REACH detection notification

REACH testing is the abbreviation of the EU regulation REGULATION CONCERNING THE REGISTRATION, EVALUATION, AUTHORIZATION AND RESTRICTION OF CHEMICALS. It is a chemical regulatory system established by the EU and implemented on June 1, 2007.

This is a regulatory proposal involving the production, trade and use safety of chemicals. The purpose of the regulation is to protect human health and environmental safety, maintain and improve the competitiveness of the European Union chemical industry, as well as the innovative ability to develop non-toxic and harmless compounds, prevent market fragmentation, increase the transparency of the use of chemicals, promote non-animal experiments, and pursue social sustainable development. REACH has established the idea that society should not introduce new materials, products or technologies if their potential hazards are uncertain.

REACH detection notification

The candidate list in Annex XIV of REACH Regulation is the SVHC list. REACH Regulation stipulates that the manufacturer or importer of substances of high concern (SVHC) that meet the following two conditions shall notify ECHA:

● The total content of SVHC substances in the article exceeds 1 t/y/manufacturer or importer;

● The total content of SVHC in the article exceeds 0.1% by mass fraction.


Who needs SVHC notification


● EU manufacturers


● EU importers

● Non-EU manufacturers (must entrust the only representative OR)

When to notify

● For substances listed in the SVHC list before December 1, 2010, the notification must be submitted within 6 months from June 1, 2011;

● For substances listed in the SVHC list after December 1, 2010, the notification must be submitted within 6 months from the date of publication. SVHC list release process

SVHC is expected to produce 1400 to 2000 items.

● The first batch of SVHC lists (15 items) was officially published and took effect in October 2008

● The second batch of SVHC lists (14 items) came into force in January 2010

● On March 30, 2010, acrylamide was listed in SVHC list

● The third batch of SVHC list (8 items) was officially published and took effect on June 18, 2010

● The fourth batch of SVHC lists (8 items) came into force on December 15, 2010

● SVHC's fifth batch list (7 items) was officially released and took effect on June 20, 2011

● SVHC's sixth batch list (20 items) was officially released and took effect on December 19, 2011

On June 18, 2012, EHCA issued the seventh batch of SVHC list (13 items), totaling 86 items;

On June 18, 2012, EHCA integrated the aluminum silicate refractory ceramic fiber (Al-RCF) and aluminum zirconia silicate refractory ceramic fiber (ZrAl-RCF) in the second batch into the sixth batch of SVHC list, reducing the second batch of SVHC list to 13 items; The total list is 84 items;


On December 19, 2012, ECHA issued the eighth batch of SVHC lists (54 items), a total of 138 items;

On June 30, 2013, ECHA issued the ninth batch of SVHC lists (6 items), totaling 144 items;

On December 16, 2013, ECHA issued the tenth batch of SVHC list (7 items), totaling 151 items;

On June 16, 2014, ECHA issued the eleventh batch of SVHC lists (4 items), totaling 155 items;

On December 17, 2014, ECHA issued the 12th batch of SVHC list (6 items), totaling 161 items;

On June 15, 2015, ECHA issued the 13th batch of SVHC list (2 items), totaling 163 items;

On December 17, 2015, ECHA issued the 14th batch of SVHC list (5 items), totaling 168 items;

On June 20, 2016, ECHA issued the 15th batch of SVHC list (1 item), totaling 169 items;

On January 12, 2017, ECHA issued the 16th batch of SVHC list (4 items), a total of 173 items;

On July 10, 2017, ECHA released the seventeenth batch of SVHC list (1 item), totaling 174 items. At the same time, for the five substances listed in the list, bisphenol A, BBP, DEHP, DBP and DIBP, the endocrine disrupting properties of human body were added;

On January 15, 2018, ECHA issued the 18th batch of SVHC list (7 items), a total of 181 items. At the same time, bisphenol A in the list has been updated.

On June 27, 2018, ECHA issued the 19th SVHC list (10 items), a total of 191 items.

On January 15, 2019, ECHA issued the 20th batch of SVHC list (6 items), a total of 197 items.

On July 16, 2019, EHCA issued the 21st batch of SVHC list (4 items), totaling 201 items.

On January 16, 2020, EHCA issued the 22nd batch of SVHC lists (4 items), totaling 205 items.

Why SVHC notification

The EU implements REACH regulations on products circulating in China. The products in the EU must fulfill the obligations of REACH regulations before they can be legally produced or imported. Countries have adopted strict supervision and punishment measures for REACH legislation. EU customs can conduct REACH compliance review. If the REACH regulations are violated, they will face product recall, fines and even imprisonment.

Responsibilities and obligations of enterprises

·When selling as a substance, it is necessary to provide SDS (safety data sheet) to downstream users.

·As a substance in the mixture (preparation), when the content of this substance is ≥ 0.1%, SDS needs to be provided to downstream users.

·When the SVHC mass percentage in the article is more than 0.1%, the recipient of the article or the consumer must be provided with sufficient information available free of charge within 45 days, including the name of the substance and its content.

·For SVHC listed before December 1, 2010, if the mass percentage concentration in the article is more than 0.1% and the total amount is more than 1 ton/year, the obligation to notify ECHA must be completed on June 1, 2011. SVHC listed after December 1, 2010, if meeting the notification conditions, must complete the notification within 6 months after listing.

limit

If the product contains any restricted substances, which are listed in Annex XVII of the Regulation, it must be used according to the restricted conditions. The restricted methods include use restrictions and dosage restrictions.


Restrictions on the manufacture, placing on the market and use of certain hazardous substances, mixtures and articles

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