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Oxalate Homeostasis in Non-Stone-Forming Chronic Kidney Disease: A Review of Key Findings and Perspectives

doi: 10.1016/j.ijantimicag.2004.09.020

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Medical Device Application Technical Files such as device description, intended purpose, design and manufacturing details, labeling, risk assessment, and clinical evidence (if required) Australian Declaration of Conformity Manufacturer’s Evidence (CE Certificate) Appointment of Australian Sponsor Pre-Market Evaluation For higher-risk device classes such as Class IIb and III, a pre-market evaluation may be required

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