TUGI - Promoton s.ro. products
TUGI - Injectable Drugs In the Treatment and Prevention of Thrombosis
TUGIs are approved for adult users only. TUGIs are not intended for unlisted medications (e.g., diabetes medications). TUGIs’ innovation is protected by a number of registered industrial designs, patents, and trademarks in the EU, USA, Canada, Switzerland, Japan, Republic of Korea, India, Norway, Russia, and other countries. The principle, design, and names of these products are protected. In the EU, TUGI is classified as a risk class I, non-sterile, non-measuring medical device (according to Annex VII of European Regulation 2017/745). The declaration of conformity guarantees compliance with EN ISO 14971:2012, EN ISO 10993-5:2009, EN ISO 10993-10:2013 from the manufacturer.
TUGI - Injectable Drug Copaxone Used in the Treatment of Multiple Sclerosis
TUGIs are approved for adult users only. TUGIs are not intended for unlisted medications (e.g., diabetes medications). TUGIs’ innovation is protected by a number of registered industrial designs, patents, and trademarks in the EU, USA, Canada, Switzerland, Japan, Republic of Korea, India, Norway, Russia, and other countries. The principle, design, and names of these products are protected. In the EU, TUGI is classified as a risk class I, non-sterile, non-measuring medical device (according to Annex VII of European Regulation 2017/745). The declaration of conformity guarantees compliance with EN ISO 14971:2012, EN ISO 10993-5:2009, EN ISO 10993-10:2013 from the manufacturer.
TUGI A Reliable Assistant
TUGIs are approved for adults. TUGIs are not intended for unlisted medications (e.g., diabetes medications). TUGIs‘ innovation is protected by a number of registered industrial designs, patents, and trademarks in the EU, USA, Canada, Switzerland, Japan, Republic of Korea, India, Norway, Russia, and other countries. The principle, design, and names of these products are protected. In the EU, TUGI is classified as a risk class I, non-sterile, non-measuring medical device (according to Annex VII of European Regulation 2017/745). The declaration of conformity guarantees compliance with EN ISO 14971:2012, EN ISO 10993-5:2009, EN ISO 10993-10:2013 from the manufacturer.