My bookmarksSign up free
Source

Commission Implementing Regulation (EU) 2020/1147 of 31 July 2020 granting a Union authorisation for the single biocidal product ‘ClearKlens product based on IPA’ (Text with EEA relevance)

Commission Implementing Regulation (EU) 2020/1147 of 31 July 2020 granting a Union authorisation for the single biocidal product ‘ClearKlens product based on IPA’ (Text with EEA relevance)

Implementing Regulation (EU) 2020/1147 · Regulation · 3 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Article 1

Open ↗

A Union authorisation with authorisation number EU-0022128-0000 is granted to Diversey Europe Operations B.V. for the making available on the market and use of the single biocidal product ‘ClearKlens product based on IPA’ in accordance with the summary of the biocidal product characteristics set out in the Annex. The Union authorisation is valid from 24 August 2020 until 31 July 2030.

Article 2

Open ↗

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .

Supplementary provisions

Summary of product characteristics for a biocidal product

ANNEXSupplementary provisions

Open ↗

ANNEX Summary of product characteristics for a biocidal product ClearKlens product based on IPA Product type 2 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Authorisation number: EU-0022128-0000 R4BP asset number: EU-0022128-0000 1.    ADMINISTRATIVE INFORMATION 1.1.    Trade name(s) of the product Trade name(s) ClearKlens IPA ClearKlens IPA 70 % ClearKlens IPA 70 % v/v ClearKlens IPA VH1 ClearKlens IPA Airless ClearKlens IPA Pouch ClearKlens IPA Non Sterile ClearKlens IPA Non Sterile VH1 ClearKlens IPA SS ClearKlens IPA SS VH1 ClearKlens IPA RTU ClearKlens IPA RTU VH1 Texwipe® Sterile 70 % Isopropanol VH01 ClearKlens IPA 1.2.    Authorisation holder Name and address of the authorisation holder Name Diversey Europe Operations B.V. Address Maarssenbroeksedijk 2, 3542 DN, Utrecht, Netherlands Authorisation number EU-0022128-0000 R4BP asset number EU-0022128-0000 Date of the authorisation 24.8.2020 Expiry date of the authorisation 31.7.2030 1.3.    Manufacturer(s) of the product Name of manufacturer Diversey Europe Operations B.V. Address of manufacturer Maarssenbroeksedijk 2, 3542 DN Utrecht Netherlands Location of manufacturing sites Avenida Conde Duque 5, 7 y 9; Poligono Industrial La Postura, 28343 Valdemoro (Madrid) Spain Strada Statale 235, 26010 Bagnolo Cremasco (CR) Italy Cotes Park Industrial Estate, DE55 4PA Somercotes Alfreton United Kingdom Rembrandtlaan 414, 7545 ZW Enschede Netherlands Morschheimer Strasse 12, 67292 Kirchheimbolanden Germany Name of manufacturer Multifill BV Address of manufacturer Constructieweg 25a, 3640 AJ Mijdrecht Netherlands Location of manufacturing sites Constructieweg 25a, 3640 AJ Mijdrecht Netherlands Name of manufacturer Flexible Medical Packaging Ltd Address of manufacturer Unit 8, Hightown, White Cross Industrial Estate, LA1 4XS Lancaster, Lancashire United Kingdom Location of manufacturing sites Unit 8, Hightown, White Cross Industrial Estate, LA1 4XS Lancaster, Lancashire United Kingdom Name of manufacturer Ardepharm Address of manufacturer Les Iles Ferays, 07300 Tournon-sur-Rhône France Location of manufacturing sites Les Iles Ferays, 07300 Tournon-sur-Rhône France Name of manufacturer Entegris Cleaning Process (ECP) S.A.S Address of manufacturer 395 rue Louis Lépine, 34000 Montpellier France Location of manufacturing sites 395 rue Louis Lépine, 34000 Montpellier France 1.4.    Manufacturer(s) of the active substance(s) Active substance Propan-2-ol Name of manufacturer INEOS Solvents GmbH Address of manufacturer Anckelmannsplatz, D-20537 Hamburg Germany Location of manufacturing sites Shamrockstrasse 88, D-44623 Herne Germany Römerstrasse 733, D-47443 Moers Germany Active substance Propan-2-ol Name of manufacturer Shell Chemicals Europe B.V. Address of manufacturer Postbus 2334, 3000 CH Rotterdam Netherlands Location of manufacturing sites Vondelingenweg 601, 3196 KK Rotterdam-Pernis Netherlands Active substance Propan-2-ol Name of manufacturer Exxon Mobil Chemicals Address of manufacturer Hermeslaan 2, 1831 Machelen Belgium Location of manufacturing sites 4045 Scenic Highway, LA 70805 Baton Rouge United States Southampton, SO45 1TX Hampshire United Kingdom 2.    PRODUCT COMPOSITION AND FORMULATION 2.1.    Qualitative and quantitative information on the composition of the product Common name IUPAC name Function CAS number EC number Content (%) Propan-2-ol   Active Substance 67-63-0 200-661-7 63,1 2.2.    Type of formulation AL – Any other liquid 3.    HAZARD AND PRECAUTIONARY STATEMENTS Hazard statements Highly flammable liquid and vapour. Causes serious eye irritation. May cause drowsiness or dizziness. Repeated exposure may cause skin dryness or cracking. Precautionary statements Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. – No smoking. Avoid breathing spray. Wash hands thoroughly after handling. Store in a well-ventilated place. Keep cool. Dispose of contents in accordance with local regulations. Dispose of container in accordance with local regulations. IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water. In case of fire: Use alcohol-resistant foam to extinguish. 4.    AUTHORISED USE(S) 4.1.    Use description Table 1. Use # 1 – PT02: Non-porous hard surface disinfectant – professionals – mopping Product type PT02 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Where relevant, an exact description of the authorised use Not relevant Target organism(s) (including development stage) Bacteria Yeasts Field(s) of use Indoor Ready to use product for the disinfection of cleaned non-porous hard surfaces in pharmaceutical and cosmetics manufacturing facilities with air change rate of 60 per hour or more and in clean rooms with air change rate of 150 per hour or more. Application method(s) Disinfection using a mop — Application rate(s) and frequency Apply 18,4 mL product/m 2 surface. Category(ies) of users Professional Pack sizes and packaging material Containers (High Density PolyEthylene (HDPE), Polypropylene (PP), Polyethylene (PE)): 1–20 L 4.1.1.    Use-specific instructions for use Ready to use product for the disinfection of non-porous hard surfaces. Clean and dry the surface before disinfection. Wet the mop with the disinfectant and mop the surface. Wet the surface completely. Allow to take effect for at least 30 seconds. Used mops must be stored in a closed container. 4.1.2.    Use-specific risk mitigation measures Apply the product only in a sufficiently ventilated room. The minimum air change rates required are: — 60/h in pharmaceutical and cosmetics manufacturing facilities, — 150/h in cleanrooms. Do not use more than 18,4 mL product/m 2 . 4.1.3.    Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment See general directions for use. 4.1.4.    Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use. 4.1.5.    Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 4.2.    Use description Table 2. Use # 2 – PT02: Non-porous hard surface disinfectant – professionals – cloth Product type PT02 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Where relevant, an exact description of the authorised use Not relevant Target organism(s) (including development stage) Bacteria Yeasts Field(s) of use Indoor Ready to use product for the disinfection of cleaned non-porous hard surfaces in laboratories with air change rate of 8 per hour or more, in pharmaceutical and cosmetics manufacturing facilities with air change rate of 60 per hour or more and in clean rooms with air change rate of 150 per hour or more. Application method(s) Disinfection using a cloth Application rate(s) and frequency Apply 18,4 mL product/m 2 surface. Category(ies) of users Professional Pack sizes and packaging material — Containers (High Density PolyEthylene (HDPE), Polypropylene (PP), Polyethylene (PE)): 1–20 L — Containers (HDPE, PP, PE) with a pump: 200 L (cleanroom only) — Intermediate bulk containers (IBCs) with a pump (HDPE, PP, PE): 950 and 1 000 L (cleanroom only) 4.2.1.    Use-specific instructions for use Ready to use product for the disinfection of non-porous hard surfaces. Clean and dry the surface before disinfection. Wet the cloth with the disinfectant and wipe the surface. Wet the surface completely. Allow to take effect for at least 30 seconds. In cleanrooms, the exact amount of required product can also be dispensed either using a low flow-rate spray lance or into a bucket via a system of pipes. Used cloths must be disposed of in a closed container. 4.2.2.    Use-specific risk mitigation measures Apply the product only in a sufficiently ventilated room. The minimum air change rates required are — 8/h in laboratories, — 60/h in pharmaceutical and cosmetics manufacturing facilities, — 150/h in cleanrooms. Do not use more than 18,4 mL product/m 2 . The following personal risk mitigation measure can be applied for wiping disinfection unless it can be replaced by technical and/or organisational measures: Wear eye protection during handling of the product. 4.2.3.    Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment See general directions for use. 4.2.4.    Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use. 4.2.5.    Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 4.3.    Use description Table 3. Use # 3 – PT02: Non-porous hard surface disinfectant – professionals – spraying Product type PT02 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Where relevant, an exact description of the authorised use Not relevant Target organism(s) (including development stage) Bacteria Yeasts Field(s) of use Indoor Ready to use product for the disinfection of cleaned non-porous hard surfaces in laboratories with air change rate of 8 per hour or more, in pharmaceutical and cosmetics manufacturing facilities with air change rate of 60 per hour or more and in clean rooms with air change rate of 8, 60 or 150 per hour or more. Application method(s) Disinfection using a trigger spray Wiping optional to spread the product. Application rate(s) and frequency Apply 18,4 mL product/m 2 surface. Category(ies) of users Professional Pack sizes and packaging material — Trigger spray pouch (PE): 0,9 – 20 L — Bag in bottle (multilayer coextruded five-layer Ethylene vinyl acetate (EVA)/EVA/Polyvinylidene dichloride (PVDC)/EVA/EVA bag in a HDPE, PP or PE bottle): 0,9–2 L — Trigger Spray bottle (HDPE, PP, PE): 0,5–1,5 L — Airless trigger spray bottle (Low-density polyethylene (LDPE)): 0,25–1L 4.3.1.    Use-specific instructions for use Ready to use product for the disinfection of non-porous hard surfaces. Clean and dry the surface before disinfection. Spray the surface, wipe if necessary to spread the product. Wet the surface completely. Allow to take effect for at least 30 seconds. Used cloths must be disposed in a closed container. Number of applications per type of packaging, necessary to obtain an application rate of 18,4 mL product/m 2 surface: — Trigger spray pouch: apply 19 sprays/m 2 surface, — Sterile trigger (bag in bottle): apply 16 sprays/m 2 surface, — Trigger spray bottle: apply 14 sprays/m 2 surface, — Airless trigger spray bottle: apply 21 sprays/m 2 surface. 4.3.2.    Use-specific risk mitigation measures Apply the product only in a sufficiently ventilated room. The minimum air change rates required are — 8/h in laboratories, — 60/h in pharmaceutical and cosmetics manufacturing facilities, — 150/h in cleanrooms. Do not use more than 18,4 mL product/m 2 . 4.3.3.    Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment See general directions for use. 4.3.4.    Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use. 4.3.5.    Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 4.4.    Use description Table 4. Use # 4 – PT02: Non-porous glove disinfectant – professionals – non-porous glove disinfection Product type PT02 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Where relevant, an exact description of the authorised use Not relevant Target organism(s) (including development stage) Bacteria Yeasts Field(s) of use Indoor Ready to use product for the disinfection of clean non-porous gloves in laboratories with air change rate of 8 per hour or more, in pharmaceutical and cosmetics manufacturing facilities with air change rate of 60 per hour or more and in clean rooms with air change rate of 150 per hour or more. Application method(s) Disinfection of non-porous gloves Application rate(s) and frequency Apply 3 mL of product to gloved hands. Category(ies) of users Professional Pack sizes and packaging material Automatic dosing: — Containers (HDPE, PP, PE): 1–20 L — Containers (HDPE, PP, PE) with a pump: 200 L (cleanrooms only) — IBCs with a pump (HDPE, PP, PE): 950 and 1 000 L (cleanrooms only) Manual dosing: — Trigger spray pouch (PE): 0,9–20 L — Bag in bottle (multilayer coextruded five-layer EVA/EVA/PVDC/EVA/EVA bag in a HDPE, PP or PE bottle): 0,9–2 L — Trigger spray bottle (HDPE, PP, PE): 0,5–1,5 L — Airless trigger spray bottle (LDPE): 0,25–1 L 4.4.1.    Use-specific instructions for use Ready to use product for the disinfection of non-porous gloves. Automatic and manual dosing: Apply 3 mL of the product directly on clean gloved hands, distribute evenly and make sure to wet the surface completely. Allow to take effect for at least 30 seconds. Number of applications per type of packaging, necessary to apply 3 mL of product on clean gloved hands: — Trigger spray pouch: apply 3 sprays of the product on two hands, — Sterile trigger (bag in bottle): apply 3 sprays of the product on two hands, — Trigger spray bottle: apply 3 sprays of the product on two hands, — Airless trigger spray bottle: apply 4 sprays of the product on two hands. 4.4.2.    Use-specific risk mitigation measures Apply the product only in a sufficiently ventilated room. The minimum air change rates required are — 8/h in laboratories, — 60/h in pharmaceutical and cosmetics manufacturing facilities, — 150/h in cleanrooms. 4.4.3.    Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment See general directions for use. 4.4.4.    Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use. 4.4.5.    Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 5.    GENERAL DIRECTIONS FOR USE   ( 1 ) 5.1.    Instructions for use See use specific instructions. 5.2.    Risk mitigation measures Wear new protective chemical resistant gloves during product handling phase (glove material to be specified by the authorisation holder within the product information). Avoid contact with eyes. 5.3.    Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment Inhalation: May cause drowsiness or dizziness. Eye contact: Causes severe irritation. IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTRE, doctor or physician if you feel unwell. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If irritation occurs and persists, get medical attention. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. Get medical attention or advice if you feel unwell. Environmental precautions: The product should not reach sewage water or drainage ditch undiluted or unneutralised. Do not allow the product to enter drainage system, surface or ground water. Dilute with plenty of water. Methods and material for containment and cleaning up. Absorb the product with liquid-binding material (sand, diatomite, universal binders, sawdust). 5.4.    Instructions for safe disposal of the product and its packaging The product and its container must be disposed of in a safe way, in compliance with any relevant legislation on the disposal of hazardous waste. Dispose of or incinerate in accordance with the local regulations. 5.5.    Conditions of storage and shelf-life of the product under normal conditions of storage 2 years shelf-life. Keep only in original packaging. Store away from direct sunlight and below 30 °C. Store in a closed container. 6.    OTHER INFORMATION The product contains propan-2-ol (CAS No: 67-63-0), for which a European reference value of 129,28 mg/m 3 for the professional user was agreed and used for the risk assessment of the product. ( 1 )   Instructions for use, risk mitigation measures and other directions for use under this section are valid for all authorised uses.

Other acts of the same type
Council Implementing Regulation (EU) 2025/2471 of 4 December 2025 implementing Regulation (EU) 2020/1998 concerning restrictive measures against serious human rights violations and abusesCommission Delegated Regulation (EU) 2026/83 of 4 December 2025 amending Delegated Regulation (EU) 2016/1675 to add Bolivia and the British Virgin Islands to the list of high-risk third countries which have provided a written high-level political commitment to address the identified deficiencies and have developed an action plan with the FATF, and to remove Burkina Faso, Mali, Mozambique, Nigeria, South Africa and Tanzania from that listCommission Implementing Regulation (EU) 2025/2432 of 3 December 2025 making imports of certain cold-rolled flat steel products originating in India, Japan, Taiwan, Türkiye and Vietnam subject to registration with a view to allowing the levy of anti-dumping duties on the imports subject to registrationCommission Implementing Regulation (EU) 2025/2496 of 3 December 2025 on the registration of the geographical indication Istarski ovčji sir / Istrski ovčji sir (PDO) in the Union register of geographical indications pursuant to Regulation (EU) 2024/1143 of the European Parliament and of the CouncilCommission Delegated Regulation (EU) 2026/46 of 3 December 2025 amending Delegated Regulation (EU) 2016/1675 to add Russia to the list of high-risk third countries with strategic deficienciesCommission Delegated Regulation (EU) 2026/326 of 3 December 2025 amending Delegated Regulation (EU) 2023/332 supplementing Regulation (EU) 2019/818 of the European Parliament and of the Council as regards determining cases where identity data are considered as same or similar for the purpose of the multiple identity detectionCommission Delegated Regulation (EU) 2026/327 of 3 December 2025 amending Delegated Regulation (EU) 2023/333 supplementing Regulation (EU) 2019/817 of the European Parliament and of the Council as regards determining cases where identity data are considered as same or similar for the purpose of the multiple identity detectionCommission Implementing Regulation (EU) 2025/2444 of 2 December 2025 amending Implementing Regulation (EU) 2023/2058 as regards the special rate of official controls for the entry into Northern Ireland from other parts of the United Kingdom of consignments of certain retail goodsCommission Regulation (EU) 2025/2481 of 2 December 2025 amending Regulation (EU) 2024/1834 as regards definitions, transitional provisions, verification tolerances, test results corrections and other provisions that relate to fan speedCommission Delegated Regulation (EU) 2025/2487 of 2 December 2025 amending Directive 2009/81/EC of the European Parliament and of the Council in respect of the thresholds for supply, service and works contractsCommission Implementing Regulation (EU) 2025/2408 of 1 December 2025 amending Implementing Regulation (EU) 2023/1134 on measures to prevent the introduction into, establishment and spread within the Union territory of Spodoptera frugiperda (Smith) with regard to the period of application of certain provisionsCommission Implementing Regulation (EU) 2025/2409 of 1 December 2025 making imports of PET spunbond originating in the People’s Republic of China subject to registration

Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

Contents

What to look at next