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Terms and Conditions

Terms and Conditions

Copyrights on the entire content are entirely owned by S.C. Tensa Art Design SRL and can not be used or copied without the written permission of the owner.

Those who access this website have the following rights:

• Exploring the content

• Reproducing, translating or using published information only with the agreement of the source;

• Inserting links to this website (when the links are contained in commercial or advertising websites, a new window will be opened to view the site;

• The person who bases his / her decisions, actions or inaction on the information contained on this website assumes full responsibility for any losses incurred.

• The photos presented are for information and may contain accessories not included in the standard product package.

We reserve the right to refuse to collaborate with clients who have inappropriate behaviour or uncivilized language.

Any attempt of unauthorized access to the site and any attempted fraud will be reported to the authorities.

Any conflict between S.C. Tensa Art Design SRL and its clients are tried to settle amicably by agreement between the two parties, and if this is not possible, the legal provisions on the Romanian territory will apply in this area and the resolution of the conflicts is the jurisdiction of the courts authorized from the territory of Romania.

Any attempt to access another user's personal data, modify the content of or affect the performance of the server running the S.C. Tensa Art Design SRL, will be considered a fraud attempt of the IT systems. Tensa Art Design SRL and brings with it the criminal investigation against the same or those who try / have tried this fact.

For complaints, please report any copyright infringement reported to the site at

The products marketed by are new in the original packaging of the producer and are accompanied by the fiscal invoice at the time of delivery / delivery.

Exclusion of liability:

We do not assume responsibility for malfunction, viruses, damage caused by system errors, following access to our site.


By placing an order through our site, you warrant that:

- You are legally capable of entering into binding contracts
- You are at least 18 years old
- You are resident in one of the Serviced Countries
- You buy our products for yourself, or if for somebody else then the contact lenses should have been chosen by a specialist
- You conduct regular check-ups in accordance with your optician's recommendations
- You ordered from us only the recommended lenses by a specialist, and the conducted ophthalmological control confirmed the use of the chosen lenses. Also, it should be noted that it is important to have the control done, with a maximum one year before purchasing the lenses. - You order contact lanses that is sufficient for no more than 1 year of use. - You performed a medical check before ordering contact lenses for the first time or changing the type of contact lenses you use.

OPINIONS AND CERTIFICATIONS sells original products, sealed to CE standards. The products are ISO 9001 certified internationally and endorsed in Romania by the Ministry of Health.

Contact lenses with dioptres are medical devices. Marketing of medical devices (in specialized stores or online) is subject to the legal rules established by the Ministry of Health.

Marketing of these products without authorization from the Ministry of Health is strictly forbidden. The legal provisions apply to both legal entities and individuals. All medical devices must be notified to the Ministry of Health.

Contact lenses are medical devices of category IIB; maintenance and cleaning solutions are in category IIB.

The following laws regulate the commerce with medical devices: Law 176/2000, Health Minister Order No. 253/2010, GD 54/2009.

Here are some articles in the current legislation. If you want to study all the laws, you can find them on the health ministry's website, to the chapter "medical devices".

Our facility is licensed to sell contact lenses.

Please note: do not buy contact lenses from unauthorized economic agents; you risk your health!

DECISION No. 54 of 29 January 2009 on the conditions for the placing on the market of medical devices.

For the purpose of this judgment, the terms and expressions below are defined as follows:

1. medical device - any instrument, apparatus, equipment, software, material or other article used separately or in combination, including the software intended by its manufacturer, to be specifically used for diagnostic and / or therapeutic purposes and necessary the proper functioning of the medical device, intended by the manufacturer to be used for human beings for the purpose of:

c) investigation, replacement or modification of anatomy or physiological process;

1.2. Invasive devices:

Invasive device - the device that is inserted wholly or partly into the body either through an anatomical or body surface.

4.3. Rule 15

All devices intended for use in disinfecting, cleaning, rinsing or, as the case, contact lenses hydrating are included in Class IIb.

LAW NO. 176 FROM 18 OCTOBER 2000

ART. 1

(1) This law establishes the legal and institutional framework for the control of medical devices, active implantable medical devices, in vitro diagnostic medical devices, put into service and used, called medical devices, as well as control of the marketing, distribution and provision of services in the field of medical devices.

ART. 3

The activities of marketing, distribution and provision of services in the field of medical devices are carried out in compliance with the provisions of the present law and the applicable methodological norms, approved by order of the Minister of Health.

(2) The activities provided in paragraph (1) are subject to endorsement control. Exceptions to this requirement are the activities carried out by the manufacturer of the medical devices which are the subject of these activities.

(3) The notice provided in paragraph (2) shall be issued by the Ministry of Health, in compliance with the applicable methodological norms, based on the assessment of the competence and capability of the natural or legal persons, as the case may be, to carry out the activities for which the opinion is requested.

ART. 4

Medical devices shall be marketed, distributed, installed and maintained for use in accordance with the intended purpose only by the natural or legal persons for whom the notice referred to in Art. 3 par. (2).

ART. 12

The natural persons and legal persons performing the activities provided in art. 3 par. (1) are obliged, prior to the performance of these activities, to seek the opinion provided for in Art. 3 par. (3) and to make known to the Ministry of Health any changes to the conditions underlying this opinion.

ORDIN No. 253 of 26 March 2010 on the registration of medical devices.

The manufacturer, authorized representative of the manufacturer, importer or distributor established in Romania has the obligation to notify to the Ministry of Health the putting into service in Romania of medical devices of classes IIa, IIb and III.

National agencies

- France: ANSM
- Poland: Europejska agencja bezpieczeństwa i Zdrowia w Pracy

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