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Sponsor content
143 result(s) found, displaying 1 to 10
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - IPG Insertion Tool-23006 - Surgical procedure kit, neurosurgical, single-use, non-medicated.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - Lead Blank- 23013-050 - Surgical procedure kit, neurosurgical, single-use, non-medicated.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - Tearaway Introducer Assembly-23003-045,23003-060 - Surgical procedure kit, neurosurgical, single-use, non-medicated.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - BIOFLEX MiniPort Home - Red-light phototherapy unit, home-use.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - BIOFLEX MiniPort Professional - Phototherapy unit, red light, line-powered.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for RQSolutions Medical Devices Distribution Support - Gonioscope.
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject.
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject.
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject.
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject.