ISO9001
SA.3CC S1 24VDC
Medical Devices Directive
New European Standards for Medical Device EN7396-2
VSF.4
Best Practice Award
Open Day
(EC) 1907/2006 (REACH) Regulation
SA.3CC S1 24VDC
Medical Devices Directive
New European Standards for Medical Device EN7396-2
VSF.4
Best Practice Award
Open Day
(EC) 1907/2006 (REACH) Regulation

(EC) 1907/2006 (REACH) Regulation
News
REACH is a new European Community Regulation on chemicals and their safe use (EC 1907/2006), which entered into force on 1 June 2007. It deals with the Registration, Evaluation, Authorisation and Restriction of Chemical substances.
The REACH regulation gives greater responsibility to industry to manage the risks from chemicals: manufacturers and importers will be asked to gather and provide safety information on the properties of their chemical substances to allow their safe handling.
A process and procedures description was prepared to help industry to collect information and set out the following obligation: manufacturers and importers of substances in quantity of 1 tonne or more per year needs to register the information in a central database run by the European Chemical Agency (ECHA) in Helsinki.
DVP is neither manufacturer nor importer but "downstream user" of chemical substances regulated by REACH. So our suppliers will be required to gather and provide information concerning their registration application, registration or preregistration of their manufactured, imported and used chemical substances.
Considering the acquired information DVP informs that the supplied articles do not contain any chemical substance listed in the "Candidate List" and that DVP is cooperating with all the suppliers in order to verify the possible presence of its products in the above mentioned list.
We will inform and update you about the final examination and its results by means of our website (www.dvp.it).
The REACH regulation gives greater responsibility to industry to manage the risks from chemicals: manufacturers and importers will be asked to gather and provide safety information on the properties of their chemical substances to allow their safe handling.
A process and procedures description was prepared to help industry to collect information and set out the following obligation: manufacturers and importers of substances in quantity of 1 tonne or more per year needs to register the information in a central database run by the European Chemical Agency (ECHA) in Helsinki.
DVP is neither manufacturer nor importer but "downstream user" of chemical substances regulated by REACH. So our suppliers will be required to gather and provide information concerning their registration application, registration or preregistration of their manufactured, imported and used chemical substances.
Considering the acquired information DVP informs that the supplied articles do not contain any chemical substance listed in the "Candidate List" and that DVP is cooperating with all the suppliers in order to verify the possible presence of its products in the above mentioned list.
We will inform and update you about the final examination and its results by means of our website (www.dvp.it).
ISO9001
SA.3CC S1 24VDC
Medical Devices Directive
New European Standards for Medical Device EN7396-2
VSF.4
Best Practice Award
Open Day
(EC) 1907/2006 (REACH) Regulation
Office in France
New force in DVP
Thanks to Eng. Locatelli
MICROCOSM DVP
Milano office
Opening new headquarters in S. Pietro in Casale
Office in Spain
Office in Brasil
SA.3CC S1 24VDC
Medical Devices Directive
New European Standards for Medical Device EN7396-2
VSF.4
Best Practice Award
Open Day
(EC) 1907/2006 (REACH) Regulation
Office in France
New force in DVP
Thanks to Eng. Locatelli
MICROCOSM DVP
Milano office
Opening new headquarters in S. Pietro in Casale
Office in Spain
Office in Brasil
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