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All Mast activities are conducted in accordance with our certified Quality Management System to ensure customers receive products and service to the best possible standard.

Mast was first assessed against and certified to the ISO 9001 ‘Quality management systems’ standard in 1994 and is currently certified to ISO 9001 ‘Quality management systems - Requirements’, ISO 13485 ‘Medical devices – Quality management systems – Requirements for regulatory purposes’, European Directive 98/79/EC ‘on in vitro diagnostic medical devices’ for Annex II list B products and for ISO 13485 for the Canadian Medical Device Requirements (CMDCAS).

ISO 9001 Certificate of Approval.
ISO13485 Certificate of Approval.
European Directive 98/79/EC Certificate of Approval.
ISO13485 for the Canadian Medical Device Requirements (CMDCAS) Certificate of Approval.

All products for diagnostic use are CE marked.



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Mast Group Ltd is a market leading manufacturer and supplier of in -vitro diagnostic product solutions for the Microbiology

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