Sponsor content
2777 result(s) found, displaying 1831 to 1840
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Stereotactic surgery system, multi-purpose.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Stereotactic surgery system, multi-purpose.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - NC Euphora Rapid Exchange Balloon Dilatation Catheter - Angioplasty catheter, balloon dilatation, coronary, basic.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Pipeline Flex Embolization Device - Stent, vascular, intracranial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Cable/lead, electroencephalograph.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Evacuator, smoke, surgical.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for Medtronic Australasia Pty Ltd - Light, surgical.
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Cancellation or suspensionRegulatory action due to Pursuant to section 41GA(1)(a)(i) of the Act, there is a potential risk of death, serious illness or serious injury if the Device continues to be included in the Register and pursuant to section 41GA(I)(b) of the Act it is likely that Medtronic Australasia Pty Ltd will, within the 6 month period of suspension, be able to take the action necessary to ensure that the Device would not cause a potential risk of death, serious illness or serious injury if it were to continue to be included in the Register., effective 05/02/2018
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Cancellation or suspensionRegulatory action due to Pursuant to section 41GA(1)(a)(i) of the Act, there is a potential risk of death, serious illness or serious injury if the Device continues to be included in the Register and pursuant to section 41GA(I)(b) of the Act it is likely that Medtronic Australasia Pty Ltd will, within the 6 month period of suspension, be able to take the action necessary to ensure that the Device would not cause a potential risk of death, serious illness or serious injury if it were to continue to be included in the Register., effective 05/02/2018
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Cancellation by sponsorRequested by Medtronic Australasia Pty Ltd