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QUALITY
Medical Technologies medical equipment designing and manufacturing are directed by basic international standards requirements for medical devices:
- Europe Union directives for medical devices ECC 93/42
- International standards ISO 14971, ISO 11197, ISO 7396 and others.
Companies designing, manufacturing and services are certified to ISO 9001 and ISO 13485 requirements. Presented to the market medical devices are marked CE conformity marks.
All medical equipment presented to the consumer is 100% checked, to each device is given individual identification number, authorizing expeditiously identify possible unconformity cause and efficiently eliminate it.
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