All products shown on this website might not be available on all markets.
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Perfadex® is registered as a pharmaceutical product in Sweden. It is sold on a named clinic/named patient basis in most European countries.
Perfadex® is registered as a medical device in US, Canada and Israel.
STEEN Solution™ and Silicone Tubing Set™ are all CE-marked.
For more information on pending registrations, please contact our Regulatory Affairs Office at:
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We accept orders by phone, fax or e-mail.
If you are located in North or South America, please contact our US office. For customers in all other countries, please contact our office in Sweden.
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For some countries we work with distributors, see links below. Should your country not be in the list, please contact Vitrolife´s head quarter in Göteborg, Sweden for further guidance.
Tel: +46 31 721 80 26/49/59
Fax: +46 31 721 80 90
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| Find a distributor in your area |
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