FTM Packaging started to produce medical sterile packaging in 2010 after its experience in the sector. It realizes its production in Class 8 Clean-Room conditions with the latest technology machines. Our company, which fulfills all the requirements of TS EN 868-5 and TS EN 11607-1 standards in our products, has proven that it fulfills all the requirements of the medical device regulation with EN ISO 9001: 2015, EN ISO 13485: 2016 certificates and CE marking.

With the use of first class raw materials, we have achieved the quality of sterilization packaging in accordance with EU norms with our certificates.

FTM Packaging aims to significantly meet the demand for quality sterile barrier system packaging in the domestic sector.