THE Therapeutic Goods Administration (TGA) has opened a series of three related consultations around medical devices contacting the human body:
1. a new device classification for substances introduced into the body via a body orifice or applied to the skin
2. a device change of classification when used in direct contact with the heart, central circulatory or central nervous systems
3. a classification for human cells, tissues and organs storage solutions and IVF media - see tga.gov.au.
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