说明与适用边界
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监管定义 / Regulatory definition
The Automatic Intramuscular Stimulator is a device that aids muscle stimulation by using a method called dry needling for treatment. The device consists of a main control unit, a hand-held motor unit, and an AC power supply adapter. The motor unit has a mounted disposal syringe and a needle mounting hardware for a disposable needle, and enables the practitioner to administer treatment with less physical effort. An EMG needle is used instead of an acupuncture needle because it is less flexible than the acupuncture needle
监管信息 / Regulatory information
FDA product code: NRW
Device class: 2
Regulation: 880.5580
Specialty: General Hospital
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.

