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Focus on quality

SSI’s development, production and sales of in vitro diagnostics are quality assured and certified in accordance with ISO 9001 and ISO 13485. Products that meet the definitions in Council Directive 98/79/EC of 27 October 1998 on in vitro diagnostic medical devices are CE labeled.

Last revised 26 August 2010

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Contact

Statens Serum Institut
SSI Diagnostica
2 Herredsvejen
3400 Hillerød
Denmark

Fax: +45 4829 9179
Tel: +45 4829 9178

(inquiries)
(ordering)
www.ssi.dk/ssidiagnostica