Changes

Our official policy is to diligently follow these regulations and all our clients are recommended to follow our example in this respect.

Our official policy is to diligently follow these regulations and all our clients are recommended to follow our example in this respect.

Teltonika goes through the required certification processes as an independent manufacturer. Once the devices are safe to market, the devices are offered for sale. At this stage the set of test reports and certificates/type approvals proving the compliance with aforementioned regulations are available. Please contact your sales manager or [mailto:[email protected] contact us] to find out which rebadging options you have. To properly rebrand a device, Teltonika recommends following a procedure as described below:

Teltonika goes through the required certification processes as an independent manufacturer. Once the devices are safe to market, the devices are offered for sale. At this stage the set of test reports and certificates/type approvals proving the compliance with the aforementioned regulations are available. Please contact your sales manager or [mailto:[email protected] contact us] to find out which rebadging options you have. To properly rebrand a device, Teltonika recommends following a procedure as described below:

* Contact us with a request of Customer Specific Requirements (CRS) form. Fill in the form with a clear statement that you would like to change the trade mark and type to your own. Please also state the company name and HQ address as it will appear in the manufacturer information.

* Contact us with a request for Customer Specific Requirements (CRS) form. Fill in the form with a clear statement that you would like to change the trademark and type to your own. Please also state the company name and HQ address as it will appear in the manufacturer's information.

* We will contact the test laboratories to reissue the test reports under the client company name and issue certificates/type approvals under a new manufacturer name to avoid obstacles to rebranded product sales in the EU market.

* We will contact the test laboratories to reissue the test reports under the client company name and issue certificates/type approvals under a new manufacturer name to avoid obstacles to rebranded product sales in the EU market.

* When you are provided with the CE RED certificate, please draw up your own Declaration of Conformity and follow the CE RED requirements as listed [[#Manufacturer responsibilities according to Directive 2014/53/EU|below]].

* When you are provided with the CE RED certificate, please draw up your own Declaration of Conformity and follow the CE RED requirements as listed [[#Manufacturer responsibilities according to Directive 2014/53/EU|below]].

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When rebranding, the economic operator placing the devices under own name is considered to be a manufacturer and assumes the obligation of the manufacturer as per p. 35 of Directive 2014/53/EU.

When rebranding, the economic operator placing the devices under their own name is considered to be a manufacturer and assumes the obligation of the manufacturer as per p. 35 of Directive 2014/53/EU.

==Manufacturer responsibilities according to Directive 2014/53/EU==

==Manufacturer responsibilities according to Directive 2014/53/EU==

The key responsibilities of a manufacturer are:

The key responsibilities of a manufacturer are:

* Drawing up a Declaration of Conformity (DoC) as per requirement of Article 10.3 and according to statements of Article 18.

* Drawing up a Declaration of Conformity (DoC) as per the requirement of Article 10.3 and according to statements of Article 18.

* Supplying a copy of DoC with every item according to Article 10.9.

* Supplying a copy of DoC with every item according to Article 10.9.

* Applying CE mark according to the requirements of Regulation No. 765/2008.

* Applying CE mark according to the requirements of Regulation No. 765/2008.

* Preparing the necessary documentation as per requirement of Article 10.3 and according to statements of Article 21.

* Preparing the necessary documentation as per the requirement of Article 10.3 and according to statements of Article 21.

* Providing instructions and safety information, among which radio frequency bands and maximum power need to be indicated, according to the requirements of Article 10.8.

* Providing instructions and safety information, among which radio frequency bands and maximum power need to be indicated, according to the requirements of Article 10.8.

* Indicating a reliable point of contact as per requirement of Article 10.7.

* Indicating a reliable point of contact as per the requirement of Article 10.7.

* Providing the documents that demonstrate the conformity when requested by a competent national authority.

* Providing the documents that demonstrate the conformity when requested by a competent national authority.

* Storing the documents for 10 years after placement to the market according to the requirement of Article 10.4.

* Storing the documents for 10 years after placement to the market according to the requirement of Article 10.4.

==Manufacturer responsibilities according to Regulation No. 661/2009 and Directive 2007/46/EC==

==Manufacturer responsibilities according to Regulation No. 661/2009 and Directive 2007/46/EC==

The key responsibilites of a manufacturer are:

The key responsibilities of a manufacturer are:

* Demonstrating the type-approval in accordance to the measures and requirements of Article 4.2 of Regulation No. 661/2009.

* Demonstrating the type-approval in accordance with the measures and requirements of Article 4.2 of Regulation No. 661/2009.

* Affixing EC type approval mark on the label as per requirement of Article 19 of Directive 2007/46/EC.

* Affixing EC type-approval mark on the label as per the requirement of Article 19 of Directive 2007/46/EC.

[[Category: Frequently Asked Questions - FAQ]]

[[Category: Frequently Asked Questions - FAQ]]