Commission Implementing Regulation (EU) 2023/1105 of 6 June 2023 granting a Union authorisation for the single biocidal product ‘Superficid express WIPES’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)
Date: 2023-06-06
Institutions: Directorate-General for Health and Food Safety, European Commission
Subjects: animal health, biocide, chemical product, decontamination, food safety, market approval, public health








L_2023147EN.01006801.xml










7.6.2023   


EN


Official Journal of the European Union


L 147/68








            COMMISSION IMPLEMENTING REGULATION (EU) 2023/1105
of 6 June 2023
         
granting a Union authorisation for the single biocidal product ‘Superficid express WIPES’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
(Text with EEA relevance)


THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,


Having regard to Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (1), and in particular Article 44(5), first subparagraph, thereof,

Whereas:







(1)


On 23 April 2019, Lysoform Dr. Hans Rosemann GmbH submitted to the European Chemicals Agency (‘the Agency’) an application in accordance with Article 43(1) of Regulation (EU) No 528/2012 and Article 4 of Commission Implementing Regulation (EU) No 414/2013 (2) for authorisation of the same single biocidal product, as referred to in Article 1 of Implementing Regulation (EU) No 414/2013, named ‘Superficid express WIPES’, of product-types 2 and 4, as described in Annex V to Regulation (EU) No 528/2012. The application was recorded under case number BC-RL051111-45 in the Register for Biocidal Products (‘the Register’). The application also indicated the application number of the related reference biocidal product family ‘Knieler & Team Propanol Family’, recorded in the Register under case number BC-AQ050985-22.












(2)


The same single biocidal product ‘Superficid express WIPES’ contains propan-1-ol and propan-2-ol as the active substances, which are included in the Union list of approved active substances referred to in Article 9(2) of Regulation (EU) No 528/2012 for product-types 2 and 4.












(3)


On 8 December 2021, the Agency submitted to the Commission an opinion (3) and the draft summary of the biocidal product characteristics (‘SPC’) of ‘Superficid express WIPES’ in accordance with Article 6 of Implementing Regulation (EU) No 414/2013.












(4)


The opinion concludes that the proposed differences between the same single biocidal product and the related reference biocidal product are limited to information which can be the subject of an administrative change in accordance with Commission Implementing Regulation (EU) No 354/2013 (4), and that based on the assessment of the related reference biocidal product family ‘Knieler & Team Propanol Family’ and subject to compliance with the draft SPC, the same single biocidal product meets the conditions laid down in Article 19(1) of Regulation (EU) No 528/2012.












(5)


On 24 October 2022, the Agency transmitted to the Commission the draft SPC in all the official languages of the Union in accordance with Article 44(4) of Regulation (EU) No 528/2012.












(6)


The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for the same single biocidal product ‘Superficid express WIPES’.












(7)


The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Biocidal Products,





HAS ADOPTED THIS REGULATION:



Article 1
A Union authorisation with authorisation number EU-0027676-0000 is granted to Lysoform Dr. Hans Rosemann GmbH for the making available on the market and use of the same single biocidal product ‘Superficid express WIPES’ in accordance with the summary of the biocidal product characteristics set out in the Annex.
The Union authorisation is valid from 27 June 2023 until 31 July 2032.


Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.




This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 6 June 2023.


For the Commission


The President

Ursula VON DER LEYEN
            





(1)  
            OJ L 167, 27.6.2012, p. 1.

(2)  Commission Implementing Regulation (EU) No 414/2013 of 6 May 2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 125, 7.5.2013, p. 4).

(3)  ECHA opinion for ‘Superficid express WIPES’ of 8 December 2021, https://echa.europa.eu/opinions-on-union-authorisation.

(4)  Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 109, 19.4.2013, p. 4).




ANNEX
Summary of product characteristics for a biocidal product
Superficid express WIPES
Product type 2 - Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants)
Product type 4 - Food and feed area (Disinfectants)
Authorisation number: EU-0027676-0000
R4BP asset number: EU-0027676-0000
1.   ADMINISTRATIVE INFORMATION

1.1.   Trade name(s) of the product







Trade name(s)


Superficid express WIPES
Bactesil Wipes
IPA Express Wipes
Twoalko Express Wipes
MicrobaX Express Wipes
Alkodes Express Wipes
Septokil Express Wipes
Mastersept Express Wipes
Descoficid Wipes
Bactoficid Express Wipes
Supergerm Express Wipes
Superdes Express Wipes
APESIN express F wipes




1.2.   Authorisation holder








Name and address of the authorisation holder


Name


Lysoform Dr. Hans Rosemann GmbH




Address


Kaiser-Wilhelm-Str. 133, 12247 Berlin Germany




Authorisation number


EU-0027676-0000





R4BP asset number



EU-0027676-0000




Date of the authorisation


27 June 2023




Expiry date of the authorisation


31 July 2032




1.3.   Manufacturer(s) of the product







Name of manufacturer


Lysoform Dr. Hans Rosemann GmbH,




Address of manufacturer


Kaiser-Wilhelm-Str. 133, 12247 Berlin Germany




Location of manufacturing sites


Lysoform Dr. Hans Rosemann GmbH, Kaiser-Wilhelm-Str. 133, 12247 Berlin Germany
A.F.P. Antiseptica Forschungs- und Produktionsgesellschaft mbH, Otto-Brenner-Straße 16-18, 21337 Lüneburg Germany
Sterisol AB, Kronoängsgatan 3, S 59223 Vadstena Sweden




1.4.   Manufacturer(s) of the active substance(s)







Active substance


Propan-1-ol




Name of manufacturer


OQ Chemicals GmbH (formerly Oxea GmbH)




Address of manufacturer


Rheinpromenade 4a, 40789 Monheim am Rhein Germany




Location of manufacturing sites


OQ Chemicals Corperation (formerly Oxea Coperation), 2001 FM 3057 TX, 77414 Bay City United States













Active substance


Propan-1-ol




Name of manufacturer


BASF SE




Address of manufacturer


Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany




Location of manufacturing sites


BASF SE, Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany













Active substance


Propan-2-ol




Name of manufacturer


INEOS Solvent Germany GmbH




Address of manufacturer


Römerstrasse 733, 47443 Moers Germany




Location of manufacturing sites


INEOS Solvent Germany GmbH, Römerstrasse 733, 47443 Moers Germany
INEOS Solvent Germany GmbH, Shamrockstrasse 88, 44623 Herne Germany




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-1-ol


 


Active Substance


71-23-8


200-746-9


14,3 




Propan-2-ol


 


Active Substance


67-63-0


200-661-7


63,14 




2.2.   Type of formulation

AL - Any other liquid
3.   HAZARD AND PRECAUTIONARY STATEMENTS







Hazard statements


Highly flammable liquid and vapour.
Causes serious eye damage.
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.
Keep container tightly closed.
Avoid breathing vapours.
Use only outdoors or in a well-ventilated area.
IF INHALED:Remove person to fresh air and keep comfortable for breathing.
IF IN EYES:Rinse cautiously with water for several minutes.Remove contact lenses, if present and easy to do. Continue rinsing.
Immediately call a POISON CENTER/doctor.
Store in a well-ventilated place.Keep cool.
Store locked up.
Dispose of contents to an authorised waste collection point.




4.   AUTHORISED USE(S)

4.1.   Use description


Table 1


Use # 1 – hard non-porous small surface disinfection RTU wipes







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)


Scientific name: no data
Common name: Bacteria
Development stage: no data
Scientific name: no data
Common name: Yeasts
Development stage: no data
Scientific name: no data
Common name: Enveloped viruses
Development stage: no data




Field(s) of use


Indoor
Health care facilities and pharmaceutical and cosmetic industry, for example patient-near surrounding, working areas/desks, general equipment (excluding food contact surfaces): disinfection of small hard/non-porous surfaces
For professional use only.




Application method(s)


Method: Manual application
Detailed description:
Ready-to-use disinfectant wipes at room temperature (20±2 °C).
The surface to be disinfected is wiped and wetted with a sufficient amount of the product, ensuring complete Coverage.




Application rate(s) and frequency


Application Rate: Minimum exposure time: for the control of bacteria, yeasts and enveloped viruses: 60 sec; Make the surface completely wet.
Dilution (%): Ready-to-use product
Number and timing of application:
A reasonable frequency of disinfection in a patient’s room is 1-2 per day. Maximum number of applications is 6 per day. No safety intervals need to be considered between the application phases.




Category(ies) of users


Industrial
Professional




Pack sizes and packaging material


Dispenser of PE composite foil with screwed-in PE cap, containing 100 PP/PE wipes.




4.1.1.   Use-specific instructions for use

Surfaces should always be visibly clean prior to disinfection. Maximum number of applications is 6 per day.
4.1.2.   Use-specific risk mitigation measures

See general directions for use.
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 – hard non-porous small surface disinfection RTU wipes







Product type


PT04 - Food and feed area (Disinfectants)




Where relevant, an exact description of the authorised use


Not relevant




Target organism(s) (including development stage)


Scientific name: no data
Common name: Bacteria
Development stage: no data
Scientific name: no data
Common name: Yeasts
Development stage: no data




Field(s) of use


Indoor
Health care facilities and food industry, for example patient-near surrounding, food preparation and handling in kitchens/restaurants): disinfection of small hard/non-porous surfaces.
For professional use only.




Application method(s)


Method: Manual application
Detailed description:
Ready-to-use disinfectant wipes at room temperature (20±2 °C).
The surface to be disinfected is wetted with a sufficient amount of the product by wiping, ensuring complete coverage.




Application rate(s) and frequency


Application Rate: Minimum exposure time: for the control of bacteria and yeasts at 20°C: 60 sec; Make the surface completely wet.
Dilution (%): Ready-to-use product
Number and timing of application:
The product can be used as often as necessary. A reasonable frequency of disinfection in kitchens is 1-2 per day. No safety intervals need to be considered between the application phases.




Category(ies) of users


Industrial
Professional




Pack sizes and packaging material


Dispenser of PE composite foil with screwed-in PE cap, containing 100 PP/PE wipes.




4.2.1.   Use-specific instructions for use

Surfaces should always be visibly clean prior to disinfection.
4.2.2.   Use-specific risk mitigation measures

See general directions for use.
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.
5.   GENERAL DIRECTIONS FOR USE (1)

5.1.   Instructions for use

For professional use only.
For wipes reseal the package after opening.
5.2.   Risk mitigation measures

Avoid contact with eyes.
Keep out of reach of children
5.3.   Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment

First-aid measures general: Move the affected person away from the contaminated area. Get medical advice/attention if you feel unwell. If possible, show this sheet.
IF INHALED: Move to fresh air and keep at rest in a position comfortable for breathing. Call a POISON CENTRE or a doctor.
IF ON SKIN: Immediately wash skin with plenty of water. Thereafter take off all contaminated clothing and wash it before reuse. Continue to wash the skin with water for 15 minutes. Call a POISON CENTRE or a doctor.
IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing for at least 15 minutes. Call 112/ambulance for medical assistance.
Information to Healthcare personnel/doctor:
The eyes should also be rinsed repeatedly on the way to the doctor if eye exposure to alkaline chemicals (pH > 11), amines and acids like acetic acid, formic acid or propionic acid.
IF SWALLOWED: Immediately rinse mouth. Give something to drink, if exposed person is able to swallow. Do NOT induce vomiting. Call 112/ambulance for medical assistance.
Accidental release measures:Stop leak if safe to do so. Remove ignition sources. Use special care to avoid static electric charges. No open flames. No smoking.Prevent entry to sewers and public waters.Wipe up with absorbent material (for example cloth). Soak up spills with inert solids, such as clay or diatomaceous earth as soon as possible. Take up mechanically (sweeping, shovelling). Dispose of in accordance with relevant local regulations.
5.4.   Instructions for safe disposal of the product and its packaging

Disposal must be done according to official regulations. Do not empty into drains. Do not dispose of with domestic waste. Dispose of contents/container to an authorised waste collection point. Empty the packaging completely prior to disposal. When totally empty, containers are recyclable like any other packing.
5.5.   Conditions of storage and shelf-life of the product under normal conditions of storage
Shelf-life: 24 months
Store in dry, cool, well-ventilated area. Keep container tightly closed. Keep out of direct sunlight.
Recommended storage temperature: 0-30°C
Do not store at temperatures below 0°C
Do not store near food, drink and animal feedingstuff. Keep away from combustible material.
6.   OTHER INFORMATION



(1)  Instructions for use, risk mitigation measures and other directions for use under this section are valid for any authorised uses.