The primary target of TONOLI S.r.l.<br>is to supply the market and the customers<br>with the right products that may satisfy every kind of needs.

The top quality with the maximum flexibility and with the best quality/service ratio

Supporting the top quality with the maximum flexibility and with the best quality/service ratio, taking advantages of its dynamic Company system. TONOLI S.r.l. sets itself as point of reference in the copper tubes and capillary distribution for specific skill, product quality and service.










Technical specialized skill supporting the appropriate usage of the commercialized products.


Punctuality in respecting the contract specifications agreed with the customer.

Courtesy and professionalism

Courtesy and professionalism on the supply supporting service.


Product certifications in line with the most restrictive standard dispositions.

Product quality

Product quality, that means also the respect of the requirements of traceability, cleanliness, technical characterization, validation of the production specifications and marking.


Shipping of the material always accompanied with 3.1 certificate according to EN 10204 standard.


Knowledge and support of a producer such as FEINROHREN S.p.A. is, with an experience in production processes ranging over 50 years.

In addition to high quality copper tubes produced according to EN 12735/1, 12735/2 and capillary tube produced according to EN 12450, TONOLI S.r.l. is the unique European Company producing copper tubes for medical gas pipeline systems, for anesthetic gases scavenging and for vacuum. TONOLI S.r.l. has aligned, since the very beginning, its quality system to the requirements of the European harmonized standard EN ISO 13485:2012 for the quality systems of medical devices manufacturers.

The quality system is hence certified according to standards EN ISO 9001 and EN ISO 13485 by KIWA CERMET ITALIA S.p.A. and it includes all requirements for the compliance to the regulatory prescriptions for traceability, vigilance and post-marketing surveillance foreseen by the Directives related to medical devices.

The CE marking of the MEDICALFEIN copper tube, hard or annealed, manufactured in compliance to standard EN 13348, is performed adopting the procedure of Annex V of MDD 93/42/EEC and subsequent modifications introduced by Directive 2007/47/EC.