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active substances and suppliers

  • HSE Web Communities

    Dear Biocides active substances web community member The EU Commission is convening a meeting of the Standing Committee on Biocidal Products (SCBP) on 17 March to vote on the approval of three active substances as follows: Silicon dioxide Kieselguhr Pyrogenic synthetic amorphous silicon dioxide nano surface treated Dichlofluanid More details of these active substances and the product

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  • Candidate List substances in articles

    Candidate List substances in articles The identification of a substance as a Substance of Very High Concern (SVHC) and its inclusion in the Candidate List can trigger certain legal obligations for the importers producers and suppliers of an article that contains such a substance

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  • Renewal of approval of active substances and those which

    Under Regulation EC 1107/2009 the rules for the renewal of approval of active substances are provided in Articles 14 to 20 Sign up to become a member today! We provide year-round advice and support on all aspects of the fresh produce industry along with exclusive networking forums publications field trips group meetings conferences and events

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  • EUR

    Any manufacturing activities in relation to active substances including re-packaging re-labelling or dividing up are subject to Commission Delegated Regulation (EU) No 1252/2014 (3) and EudraLex Volume 4 Part II Additional requirements apply to the importation of active substances as laid down in Article 46b of Directive 2001/83/EC

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  • ECHA Newsletter

    The final list of active substances and suppliers will also include the date of inclusion on the list for each substance and each supplier Fees To be included in the list an application needs to be sent to ECHA through R4BP 3 and the appropriate fee must be paid within 30 days The fees can be found in the Implementing Regulation on the fees and charges available on ECHA's website Non-EU

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  • Helpdesk

    Transitional measures for biocidal products containing existing active substances in Germany According to Article 17 of Regulation (EU) No 528/2012 (BPR) biocidal products shall not be made available on the market or used unless authorised in accordance with BPR However according to Article 89 of BPR in conjunction with 28 (8) of the Chemicals Act (Chemikaliengesetz ChemG) biocidal

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  • Volume V Guidance on active substances and suppliers

    Guidance on active substances and suppliers (Article 95 list) Version 2 0 December 2014 2 Volume V: Guidance on active substances and suppliers (Art 95 list) Version 2 0 December 2014 LEGAL NOTICE This document aims to assist users in complying with their obligations under the Biocid al Products Regulation (BPR) However users are reminded that the text of the BPR is the only

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  • Active substance approval

    The assessment of active substances prior to their approval for use in biocidal products is carried out by an EU country followed by a peer review involving all EU countries coordinated by the European Chemicals Agency (ECHA) This peer review takes place within the Biocidal Products Committee (BPC) ECHA delivers an opinion to the Commission as to whether or not an active substance can be

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  • Biocidal active substances

    Biocidal active substances Only approved active substances or existing active substances that are currently under review in the EU's risk assessment programme may be used in biocidal products The European Chemicals Agency (ECHA) maintains a product type specific list of active substance suppliers Active substances may be used in products if the supplier of the active substance or

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  • COVID

    To alleviate the difficulties companies and Member State authorities may be facing during the global coronavirus pandemic ECHA is supporting EU/EEA countries and companies to ensure that disinfectants can quickly enter the market To ease the work of authorities and biocides companies looking for information on disinfectants European Chemical Agency has published lists of active substances

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  • 529 For the approval and maintenance of suppliers of

    529 For the approval and maintenance of suppliers of active substances and 529 for the approval and maintenance of suppliers of School Open University Malaysia Course Title OUM 2220 Uploaded By raaj19 Pages 57 This preview shows page 34 - 36 out of 57 pages

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  • Article 95 List of Active Substances and Suppliers

    Article 95 List of Active Substances and Suppliers 19 10 2018 revision The Article 95 list of active substances and suppliers was first published by ECHA on 24 September 2014 The most recent update was made in September 2018 Two new substances were added for product type six: sodium azide and benzyl alcohol

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  • Guidelines of 19 March 2015 on principles of Good

    on principles of Good Distribution Practice of active substances for medicinal products for human use (Text with EEA relevance) so that all the suppliers of or those supplied with an active substance can be identified Records that should be retained and be available include: (i) identity of supplier original manufacturer shipping agent and/or consignee (ii) address of supplier

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  • Guidance

    Guidance documents aim at facilitating the implementation of the legislation in ECHA's remit by describing good practice on how to fulfil the obligations They are developed with the participation of many stakeholders: industry Member States and NGOs Guidance Documents These documents have been developed with the participation of many stakeholders: Industry Member States and NGOs The

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  • PRCD

    Active Substance Suppliers (Article 95 List) The European Chemicals Agency (ECHA) is responsible for the publication of the list of relevant substances and the respective substance and product suppliers in accordance with Article 95 of the Biocidal Products Regulation (BPR) The names of the active substance suppliers can be obtained from the List of Active Substances and Suppliers Notified

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  • ECHA Newsletter

    Finding potential substances of concern – how it happens Classify and label your mixtures in time Make sure you are included in the list of biocidal active substances and suppliers Pre-submission strongly advised for biocides Union authorisation Biocidal Products Committee adopts opinions on active substances Exporters under PIC must act now Make sense of safety data sheets and

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  • Falsified Medicines Directive: Imported active

    From 2 July 2013 all active substances manufactured outside of the European Union (EU) and imported into the EU must be accompanied by a written confirmation from the competent authority of the exporting country confirming that the standards of good manufacturing practice (GMP) and control of the manufacturing plant are equivalent to those in the EU

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  • Pharmaceutical Bulk Active Substances Suppliers

    Suppliers List E-mail/RFQ Form Molecular Structure Weight Formula IUPAC Synonyms for Pharmaceutical Bulk Active Substances Skype Pharmaceutical Bulk Active Substances Suppliers Limit companies to: Worldwide USA China India EMAIL INQUIRY to 1 to 30 of 31 suppliers Page: [1] 2 Chemlyte Solutions | Address: Building B Jian Qiao Community 789 Shenhua Road Xihu District

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  • Information on biocides

    List of active substances and suppliers Information on biocides ECHA is responsible for the publication of the list of relevant substances and the respective substance and product suppliers in accordance with Article 95 of the Biocidal Products Regulation (BPR) as amended by Regulation (EU) No 334/2014 of

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  • Active ingredient

    An active ingredient is the ingredient in a pharmaceutical drug or pesticide that is biologically active The similar terms active pharmaceutical ingredient and bulk active are also used in medicine and the term active substance may be used for natural products Some medication products may contain more than one active ingredient The traditional word for the active pharmaceutical agent is

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  • LIST OF PENDING ARTICLE 95(1) APPLICATIONS

    pending Article 95(1) applications should not be confused with the list of relevant substances and suppliers ("Article 95 list") and the presence of a company (per substance/PT/role) on the list of pending applications does not guarantee that the application will be successful and that the company will ultimately be included in the Article 95 list Joint applications are not possible under

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  • Active substances in biocidal products

    Active substances used in biocidal products must be authorised within the EU before they can be put on the market Before an active substance can be authorised it must be evaluated with respect to effectiveness and impact on human health and the environment Then after active substances have been authorised biocidal products containing the substances must also be authorised

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  • Approval of active substances

    Approval of active substances A plant protection product usually contains more than one component The active component against pests/plant diseases is called "active substance" The Commission evaluates every active substance for safety before it reaches the market in a product Substances must be proven safe for people's health including their residues in food and effects on animal

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  • Active Membrane Suppliers all Quality Active Membrane

    Active Membrane Active Membrane Suppliers Directory - Find variety Active Membrane Suppliers Manufacturers Companies from around the World at modified bitumen membrane roofing ro membrane waterproofing membrane Water Treatment

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  • Guidance

    Guidance documents aim at facilitating the implementation of the legislation in ECHA's remit by describing good practice on how to fulfil the obligations They are developed with the participation of many stakeholders: industry Member States and NGOs Guidance Documents These documents have been developed with the participation of many stakeholders: Industry Member States and NGOs The

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  • Article 95 List: Non

    This news release discussing the Article 95 List is brought to you by ECHA While preparing the publication of the first EU list of biocidal active substances and suppliers namely the Article 95 list the Agency has formally agreed with the European Commission that non-EU companies participating in the EU programme to review all existing biocidal []

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Henan Tongwei

Henan Tongwei Medical Device Co., Ltd. is a branch company of Guangzhou Ningwei Technology Co., LTD., which is specialized in the production, processing, sales, research and development and service of related products and equipment in the medical device industry.

Contact Us

  • : Room 810, Block B, Jinzhonghuan Building, Zhengzhou City, Henan Province
  • : +86 19139704654
  • : [email protected]

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NIOSH N95

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BFE99 Melt Blown Fabric

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