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Our main objective is to insure the satisfaction of our customers and all the users of our products on a daily basis. This means the manufacturing of reliable, top quality, in accordance to the regulatory requirements products and the development of products and services meeting exactly their needs. DTF medical is certified NF EN ISO 13485 (2016).

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Medical products manufactured by DTF medical have a EC certificate and comply with the requirements of the directive 93/42/CEE regarding medical devices.

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Download EC conformity declarations:


Below EC certificats and conformity declarations for products distributed by DTF:

For Smartchambers:


Eco participation:
The unique identifier FR000457_05FGFN attesting to registration in the register of producers in the EEE sector, pursuant to article L.541-10-13 of the Environmental Code, has been assigned by ADEME to the company DTF medical . This identifier certifies its conformity with regard to its obligation to register in the register of producers of Electrical and Electronic Equipment and the realization of its declarations of placing on the market with Ecosystem.