PQ 845
845. Deputy Louise O'Reilly asked the Minister for Health the procedure when a device is reported to the Health Products Regulatory Authority, HPRA; if the HPRA has the power to have a medical device removed from the Irish market; if not, the reason therefor; his views on whether this is putting persons at risk; and if he will make a statement on the matter. [46976/17]
Introduced
7 November 2017
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7 November 2017
Summary
845. Deputy Louise O'Reilly asked the Minister for Health the procedure when a device is reported to the Health Products Regulatory Authority, HPRA; if the HPRA has the power to have a medical device removed from the Irish market; if not, the reason therefor; his views on whether this is putting persons at risk; and if he will make a statement on the matter. [46976/17]
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Health Products Regulatory Authority
Health Products Regulatory Authority
xml · EN · 7 November 2017
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- Official source: https://www.oireachtas.ie/en/debates/question/2017-11-07/845/
- Open data entity: https://data.oireachtas.ie/ie/oireachtas/question/2017-11-07/pq_845