In the entire manufacturing
process, the Company maintains a working standard in accordance
with the requirements of standards PN-EN ISO 9001 : 2000,
EN ISO 13485 : 2003. The medical products manufactured by
the Company are registered at the Office for Registration
of Medicinal Products, Medical Devices and Biocides.
The Management of Weber & Weber declares
that the manufactured class I products meet the requirements
of Appendix VII to Directive 93/42/EEC of 14 June 1993. The
manufactured medical products have CE and WE marking, therefore
they may be transported freely within the European Community
and used as indicated.
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