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医疗器械 · FDA 器械监管分类(非厂家操作说明书)

Nucleic Acid Amplification, Novel Influenza A Virus, A/H5 (Asian Lineage) Rna

Nucleic Acid Amplification, Novel Influenza A Virus, A/H5 (Asian Lineage) Rna

Product code NXD · Class 2 · Microbiology

说明与适用边界

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监管定义 / Regulatory definition

Novel influenza a virus reagents are used in nucleic acid amplification tests to directly detect and differentiate novel influenza a virus specific rna gene segments in human respiratory specimens or viral cultures. Detection and differentiation of specific rna gene segments aids in the diagnosis of influenza caused by novel influenza a viruses in patients with clinical and epidemiological risk of infection with these viruses. They also aid in the presumptive identification of specific novel influenza a viruses and provide epidemiological information on influenza. These reagents are primers and probes, along with a specific novel influenza virus control.

监管信息 / Regulatory information

FDA product code: NXD Device class: 2 Regulation: 866.3332 Specialty: Microbiology 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