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【CODEX】Notice on Good Manufacturing Practice for Medical Devices（7-13）- EN
【CODEX】Notice on Good Manufacturing Practice for Medical Devices（7-13）- EN

Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（1-2）-EN
Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（1-2）-EN

Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（3）-EN
Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（3）-EN

Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（4-6）-EN
Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（4-6）-EN

Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（7-9）-EN
Provisions for Medical Device Adverse Event Monitoring and Re-Evaluation（7-9）-EN

【CODEX】Guideline for Technical Review of Posterior Spinal Internal Fixation System Registration(1-5)
【CODEX】Guideline for Technical Review of Posterior Spinal Internal Fixation System Registration(1-5)

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