NOTIFICATION

Pursuant to Article 11 of Law No. 22/1997 Collection of laws that lays down technical requirements for products, the authorisation is granted by the Czech Office for Standards, Metrology and Testing (hereinafter UNMZ).

Authorized bodies ensure all the activities connected with the conformity assessment of products according to requirements of the technical regulations. The Authorised bodies become the NOTIFIED BODIES after they are notified by UNMZ to the bodies of the European Community or to the bodies of the Member States of the European Union. Based on the documents issued by the Notified bodies, the products are affixed the CE conformity marking.

Pursuant to Article 17 of Law No. 90/2016 Collection of Laws - Conformity assessment bodies are notified to the European Commission and to other Member States of the European Union by the by the Czech Office for Standards, Metrology and Testing, which is notifying authority within the meaning of harmonisation legislation of the European Union and relevant Regulations of the European Union. The Office shall notify to the European Commission and to other Member States of the European Union also significant changes relating to notifications. For these purposes, the Office uses an electronic notification tool managed by the European Commission.

NOTIFIED BODY NO. 1023

Institute for Testing and Certification a.s. Zlin, NOTIFIED BODY NO. 1023, possesses the authorities permitting to perform conformity assessment according to the following legislation:

• EC Directive 2009/48/EC
  Directive that lays down technical requirements for toys.
  
  NB 1023 notification
   
• Commission Directive 93/42/EEC
  Directive that lays down technical requirements for medical devices.
  ITC is no longer able to issue new certificates under Directive 93/42/EEC but only allowed to carry out surveillance activities for certificates validly issued under that Directive in the transitional period, as established in Article 120 of Regulation (EU) 2017/745.
  
  NB 1023 notification
  
  
• Commission Directive No. 98/79/EEC
  Directive that lays down technical requirements for in vitro diagnostic medical devices.
  
  NB 1023 notification
  
  
• Regulation 305/2011 
  Regulation that lays down technical requirements for construction products bearing the CE marking.
  
  NB 1023 notification
  
  
• Regulation (EU) 2016/425 of the European Parliament and of the Council
  Regulation that lays down the technical requirements for personal protective equipment.
  
  NB 1023 notification
   
• Directive 2014/30/EU of the European Parliament and of the Council
  Directive that lays down the technical requirements for products in terms of their electromagnetic compatibility.
  
  NB 1023 notification
   
• Directive 2014/68/EU of the European Parliament and of the Council
  Directive that lays down the technical requirements for pressure equipment.
  
  NB 1023 notification
  

NOTIFIED BODY NO. 1390

Institute for Testing and Certification a.s. Zlin, NOTIFIED BODY NO. 1390, possesses the authorities permitting to perform conformity assessment according to the following legislation:

• Regulation 305/2011 
  Regulation that lays down technical requirements for construction products bearing the CE marking.
  
  NB 1390 notification
  

AUTHORIZED BODY 212 (Czech national law)

• GO No. 163/2002
  Collection of laws that lays down requirements for selected building products
  
  authorization + online list

AUTHORIZED BODY 224 (Czech national law)

• GO No. 173/1997
  Collection of laws that lays down requirements for selected products
  
  authorization + online list
   
• GO No. 163/2002
  Collection of laws that lays down requirements for selected building products
  
  authorization + online list

RELATED SERVICES provide by NOTIFIED BODY NO. 1023

• Toys - EC Directive 2009/48/EC
• Personal protective equipment - Council Directive 89/686/EEC
• Electromagnetic compatibility - Directive 2014/30/EU of the European Parliament and of the Council
• Medical device - Commission Directive 93/42/EEC
• Construction products - regulation 305/2011
• In vitro diagnostic medical devices - Commission Directive No. 98/79/EEC
• Pressure equipment - Directive 2014/68/EU of the European Parliament and of the Council
• Personal protective equipment - Regulation (EU) 2016/425 of the European Parliament and of the Council

RELATED SERVICES provide by NOTIFIED BODY NO. 1390

• Construction products - regulation 305/2011

RELATED SERVICES provide by AUTHORIZED BODY 212

• GO No. 163/2002

RELATED SERVICES provide by AUTHORIZED BODY 224

• GO No. 173/1997
• GO No. 163/2002

Person responsible for accuracy of data: Ing. Tomas Vesely