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Biocidal product factsheet - Last updated: 19/06/2024

Biocidal Product details

Trade name:

Neutralac® Calci-flo Optilight

Neutralac® Q

Neutralac® Q1

Neutralac® Q2

Neutralac® Q2 DB

Neutralac® Q200

Neutralac® Q3

Neutralac® Q3-7

Neutralac® Q90

Neutralac® Q90 SR

Product-type:

PT02

Active Substance details

Substance name:

Calcium oxide/lime/burnt lime/quicklime

IUPAC name:

oxocalcium

EC number:

215-138-9

CAS number:

1305-78-8

BAS number:

1259

Authorised
map
Authorisation information

Authorisation type:

Union authorisation

Legal act:

Commission Implementing Regulation (EU) 2024/1486 of 29 May 2024 granting a Union authorisation for the single biocidal product CaO PT02 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

Opinions:

R4BP_EU_0029494_0000_Opinion.pdf (en)

Assessment reports:

1 authorisation in the product cluster
Trade name
Product-type
Market area
Authorisation holder
Authorisation number
Authorisation start
Authorisation end
SPC Decisions
Authorisation status
R4BP 3 asset
National

Neutralac® Calci-flo Optilight

Neutralac® Q

Neutralac® Q1

Neutralac® Q2

Neutralac® Q2 DB

Neutralac® Q200

Neutralac® Q3

Neutralac® Q3-7

Neutralac® Q90

Neutralac® Q90 SR
PT02

Austria

Belgium

Bulgaria

Croatia

Cyprus

Czech Republic

Denmark

Estonia

Finland

France

Germany

Greece

Hungary

Ireland

Italy

Latvia

Lithuania

Luxembourg

Malta

Netherlands

Poland

Portugal

Romania

Slovakia

Slovenia

Spain

Sweden

 Lhoist EU-0029494-0000 EU-0029494-0000 19/06/2024 30/11/2033

Single SPC  (it)

R4BP_EU_0029494_0000_Authorisation.pdf (en)

 Authorised
Union authorisation
Trade name: Neutralac® Calci-flo Optilight , Neutralac® Q , Neutralac® Q1 , Neutralac® Q2 , Neutralac® Q2 DB , Neutralac® Q200 , Neutralac® Q3 , Neutralac® Q3-7 , Neutralac® Q90 , Neutralac® Q90 SR
Authorisation number: EU-0029494-0000| Market area: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden

1 assessment record available

Union authorisation

Evaluating authority:

ECHA

Conclusion date:

31/05/2024

Validity of authorisation

Start date:

19/06/2024

End date:

30/11/2033

SPC

Single SPC  (da)