Dual Site Manufacturing Facilities


Our state-of-the-art, dual site manufacturing facilities include 3 Cleanrooms validated and maintained to ISO 7 (Class 10,000), in accordance with ISO 14644-1:1999. We are accredited to international standards ISO 9001:2008 and ISO 13485:2003 and can offer a Medical Device CE Marking service to EC Directive 93/42/EEC, giving you total confidence for medical device manufacturing and regulatory compliance.

Dual Manufacturing map