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Valeo Laboratories

Valeo Laboratories E-Liquid

Valeo Liquid

The quality of our liquids has been tested and certified as excellent by various institutes, each having
evaluated a diverse range of quality features.
EN ISO 9001 defines the requirements for a quality management system (QM system) for the case in

which an organisation must demonstrate its ability to supply products that meet the requirements of
customers as well as regulatory standards, and aim to improve customer satisfaction.
This standard gives an exemplary description of the whole quality management system and is the
basis for a comprehensive quality management system.
The ISO 13485 is an ISO standard that represents the requirements for a comprehensive management
system for the design and production of medical products. [1] The current version was published in
2003 and supersedes earlier documents such as the EN 46001 und EN 46002 (both from 1997), the ISO
13485, which was published in 1996, and the ISO 13488 (also from 1996). The DIN EN ISO 13485 is the
available standard in Germany.
The Directive 2002/95/EC on the restriction of the use of certain hazardous substances in electrical and
electronic equipment regulates the use of hazardous substances in devices and components. This
directive, which is required to be enforced and become law in each member state, is also referred to
as the RoHS or Restriction of Hazardous Substances Directive).

Valeo Cert

valeo laboratories is currently the only company, which has its e-liquids examined in batches of voluntary
checks and controls by certified and accredited laboratories in Germany.
Naturally, the latest test records are published and made available to view on our home page.

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