Changing brand on OEM devices - Revision history

Gediminas.suminas at 06:58, 14 October 2020

2020-10-14T06:58:02Z

Gediminas.suminas: Protected "Changing brand on OEM devices" ([Edit=Allow only administrators] (indefinite) [Move=Allow only administrators] (indefinite))

2020-10-14T06:57:34Z

Protected "Changing brand on OEM devices" ([Edit=Allow only administrators] (indefinite) [Move=Allow only administrators] (indefinite))

← Older revision	Revision as of 09:57, 14 October 2020
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Gediminas.suminas at 05:42, 13 July 2020

2020-07-13T05:42:31Z

← Older revision		Revision as of 08:42, 13 July 2020
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	* 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 requirement of Article 19 of Directive 2007/46/EC.

	[[Category:~~Fleet management~~ FAQ]]		[[Category: Frequently Asked Questions - FAQ]]

Airidas.S at 11:44, 19 June 2019

2019-06-19T11:44:18Z

← Older revision		Revision as of 14:44, 19 June 2019
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	* 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 to 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 requirement of Article 19 of Directive 2007/46/EC.

			[[Category:Fleet management FAQ]]

Airidas.S: Created page with "GPS trackers that are offered by us fall into a category of equipment that is required to follow CE RED (2014/53/EU) regulations. Car-mounted applications must also comply wit..."

2019-06-19T11:20:37Z

Created page with "GPS trackers that are offered by us fall into a category of equipment that is required to follow CE RED (2014/53/EU) regulations. Car-mounted applications must also comply wit..."

New page

GPS trackers that are offered by us fall into a category of equipment that is required to follow CE RED (2014/53/EU) regulations. Car-mounted applications must also comply with Regulation No. 661/2009.
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:info@teltonika.lt 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.
* 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 type approval, please be prepared to demonstrate it to the customer when required. Your brand label will already be prepared by us according to all pertaining requirements.
* Contact us for test reports if they are required by a national or accredited competent authority. These reports are available at short notice.

= CE RED =

{{ce description}}

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.

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

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

= E-Mark =
{{emark description}}

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

The key responsibilites of a manufacturer are:
* Demonstrating the type-approval in accordance to 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.

← Older revision		Revision as of 09:58, 14 October 2020
Line 2:		Line 2:
	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:info@teltonika.lt 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:info@teltonika.lt 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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	{{ce description}}		{{ce description}}

	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==
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	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.
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	==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]]