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BioWorld - Sunday, December 15, 2019
Home » Australia moves to reclassify implantable spinal devices to mirror EU device regulations
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Australia moves to reclassify implantable spinal devices to mirror EU device regulations

November 8, 2019
By Tamra Sami
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PERTH, Australia – Although medical device industry stakeholders agreed in principle with the Australian Therapeutic Goods Administration's (TGA) proposal to align its classification with the EU's for implantable spinal devices, they viewed the interpretation of the EU Medical Device Regulation (MDR) classification rule for these devices differently.
Australia Asia-Pacific BioWorld MedTech TGA Therapeutic Goods Administration

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