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医疗器械 · FDA 器械监管分类(非厂家操作说明书)

Classifier, Prognostic, Recurrence Risk Assessment, Rna Gene Expression, Breast Cancer

Classifier, Prognostic, Recurrence Risk Assessment, Rna Gene Expression, Breast Cancer

Product code NYI · Class 2 · Immunology

说明与适用边界

此页按所列地区、版本归档。标签内容可能更新,具体产品请核对原始来源;本站关联表示阅读线索,不表示药品与器械可兼容或可替换。

监管定义 / Regulatory definition

A device which uses a gene expression profile of a breast cancer tumor, from patients stage i or stage ii lymph node negative, with a tumor size of <5.0 cm, to provide a risk assessment for distant recurrence of breast cancer. The result is indicated for use only as a prognostic marker by physicians along with a number of other factors to assess the risk of recurrence of breast cancer.

监管信息 / Regulatory information

FDA product code: NYI Device class: 2 Regulation: 866.6040 Specialty: Immunology Implant flag: N Life sustaining/supporting flag: N

使用说明核对

该条目描述监管产品类别,不对应某个型号。实际操作须使用该厂家、型号和软件版本的说明书,核对预期用途、适应证、禁忌、校准、耗材兼容性、清洁灭菌、维护与报警处理。类别资料不能替代厂家使用说明。

来源、版本与许可

资料类型
FDA 器械监管分类(非厂家操作说明书)
版本
2026-10-08
获取时间
2026-10-08
许可
openFDA public data; retain original label attribution. See 查看来源 and dataset source notices. Public access does not imply approval or unrestricted rights to every submitted label.
核对原始来源