厂家直供诺诚肌电生物反馈仪MyoNet-COW,MyoNet-BOW
价格：￥ 电议
品牌名称：$brandModel.Title型号： 原产地：中国大陆 医疗器械注册号(批文)：沪械注准20222090039更新时间：2026/10/16 11:11:09
支付方式：
- 支付宝 微信 银行转账
产品完善度： 访问次数：155
企业档案
会员类型：旗舰版
已获得阿仪网信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
阿仪网旗舰版会员：1年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
参观次数：137243
手机网站：http://wap.app17.com/c174616/
旗舰版网址：http://ksdy.app17.com
详细内容
厂家直供诺诚肌电生物反馈仪MyoNet-COW,MyoNet-BOW
桂经理19117326863微xin同号
桂经理19117326863微xin同号
管理类别
第二类
型号规格
MyoNet-AOW、MyoNet-BOW、MyoNet-COW
结构及组成/主要组成成分
产品由电脑主机、显示器、打印机、电源适配器、隔离电源、数据线、反馈刺激盒、电极线、电极片（理疗电极片和理疗用电极）、电极（阴道电极水滴型、直肠电极一字型、直肠电极T字型）及软件组件（发布版本V1）组成。
适用范围/预期用途
用于对患者的体表肌电信号进行采集、分析和反馈训练，可以对患者的肌肉施加电刺激来帮助和恢复患者的肌肉功能障碍。
1 工作原理 Working Principle
中文： 设备通过体表 / 腔内电极采集人体骨骼肌表面肌电（sEMG）微弱电信号，经放大、滤波、模数转换后由软件运算解析肌电幅值变化；将肌肉收缩、松弛状态以视觉、听觉形式反馈给患者，实现主动生物反馈训练；同时可输出低频脉冲电流对神经‑肌肉进行电刺激，被动驱动肌肉收缩舒张，结合主被动模式重建、恢复受损肌肉运动控制功能，改善肌肉功能障碍。
English： The device acquires faint surface electromyography (sEMG) signals of skeletal muscles via surface or intracavitary electrodes. After amplification, filtering and A/D conversion, the software calculates and analyzes EMG amplitude variation. Muscle contraction‑relaxation status is fed back to patients visually and acoustically for active biofeedback training. Meanwhile, low‑frequency pulse current can be output for neuromuscular electrical stimulation to drive muscle contraction and relaxation passively. Combined with active‑passive modes, it reconstructs and restores impaired motor control and relieves muscular dysfunction.
2 主要功能 Main Functions
中文
双通道表面肌电信号采集、肌电评估、肌电反馈训练；支持盆底肌专项评估与训练
三种训练模式：被动电刺激训练、主动肌电生物反馈训练、主‑被动联合触发训练
内置 52 种处方刺激模式，含自由刺激、反馈触发刺激、TENS 镇痛模式
多媒体游戏式反馈训练，可视化肌电波形实时显示
、治疗处方、康复数据存储、回放、报告输出；支持单机运行；可蓝牙对接中央工作站实现多终端网络化康复管理（MyoNet‑COW）
English
Dual‑channel sEMG acquisition, EMG assessment & biofeedback training; dedicated pelvic‑floor assessment and training
Three training modes: passive electrical stimulation, active EMG biofeedback, combined active‑passive trigger training
52 preset stimulation protocols including free stimulation, trigger‑based feedback stimulation and TENS analgesic mode
Multi‑media game‑based feedback training; real‑time visual EMG waveｆorm display
Medical record, therapy protocol and rehabilitation data storage, playback & report export; standalone operation; Bluetooth‑connected central workstation for network‑based multi‑terminal rehabilitation management (MyoNet‑COW)
3 产品特点 Product Features
中文
双通道同步肌电检测评估训练，兼顾肢体肌肉与盆底肌康复
主动反馈 + 被动电刺激一体化，主被动触发联动训练
丰富预设刺激处方，多媒体游戏反馈提升患者依从性
MyoNet‑COW 支持单机 / 中央工作站组网，可实现多设备集中数据管理；MyoNet‑BOW 为基础型肌电反馈刺激机型
兼容体表理疗电极片、阴道电极、直肠电极等多种电极配件
软件具备评估模板、治疗模板，简化康复方案设置
English
Dual‑channel simultaneous EMG detection, assessment and training for limb and pelvic‑floor rehabilitation
Integrated active biofeedback & passive electrical stimulation with synchronized active‑passive trigger training
Abundant preset stimulation protocols; multi‑media game feedback improves patient compliance
MyoNet‑COW supports standalone or networked central workstation for centralized multi‑device data management; MyoNet‑BOW is basic EMG biofeedback‑stimulation model
Compatible with surface therapeutic electrodes, vaginal electrodes, rectal electrodes and other accessories
Built‑in assessment & therapy templates to simplify rehabilitation protocol configuration
4 技术参数 Technical Specifications
表格
| 项目 Item | 中文 | English |
|---|---|---|
| 显示灵敏度 Display Sensitivity | 0.05µV/div～120000µV/div，误差≤±10% | 0.05µV/div～120000µV/div, error ≤±10% |
| 幅频特性 Amplitude‑Frequency Characteristic | 0.2Hz‑10kHz | 0.2Hz‑10kHz |
| 噪声电压 Noise Voltage | ≤0.4µV(RMS) | ≤0.4µV(RMS) |
| 共模抑制比 CMRR | ≥110 dB | ≥110 dB |
| 输入阻抗 Input Impedance | ≥1000 MΩ | ≥1000 MΩ |
| 刺激输出电流 Stimulation Output Current | 0‑100 mA；0‑4mA 步长 0.01mA，误差≤±10% | 0‑100 mA; step 0.01mA within 0‑4mA, error ≤±10% |
| 脉冲频率 Pulse Frequency | 0.1‑120 Hz，误差≤±10% | 0.1‑120 Hz, error ≤±10% |
| 脉冲宽度 Pulse Width | 50‑1000 µs，误差≤±10% | 50‑1000 µs, error ≤±10% |
| 刺激极性 Stimulation Polarity | 正向、负向、双向 | Positive, negative, bidirectional |
| 单次治疗时间 Therapy Duration | 5‑40 min 可调 | Adjustable 5‑40 min |
| 软件版本 Software Version | V1 | V1 |
硬件组成：主机、主控盒、刺激盒、放大采集盒、电极线缆、体表电极、可选腔内电极、电源适配器；COW 可配台车、显示器、打印机、中央工作站；BOW 为基础配置。
5 使用方法 Operation Method
中文
术前准备：检查设备、线缆、电极完好；清洁患者皮肤；按需选择体表电极或阴道 / 直肠腔内电极，规范安放电极。
开机，新建 / 调取患者，选择评估程序，执行肌电基线评估，记录肌肉静息、收缩肌电基线数据。
根据评估结果选择治疗模式：被动电刺激模式 / 主动生物反馈模式 / 主被动触发模式；选取对应刺激处方，设置刺激参数、治疗时长。
告知患者配合训练：主动模式下跟随视听反馈做肌肉收缩‑放松训练；被动模式由设备输出电流刺激肌肉。
治疗结束自动停止，保存本次康复数据，输出评估报告；取下电极，清洁电极及接触部位；设备关机收纳。
MyoNet‑COW 可蓝牙连接中央工作站实现数据上传与多病例管理。
医疗机构由经培训康复医师 / 治疗师操作。
English
Preparation: Inspect device, cables and electrodes. Clean patient skin. Apply surface electrodes or vaginal/rectal intracavitary electrodes properly.
Power‑on; create or recall patient medical record; run assessment program to acquire baseline sEMG data at rest and during muscle contraction.
Select therapy mode according to assessment result: passive stimulation / active biofeedback / combined trigger mode; choose preset protocol, configure stimulation parameters and therapy duration.
Instruct patient for cooperation: perｆorm contraction‑relaxation following audio‑visual feedback under active mode; muscle is driven by device‑output current under passive mode.
Session stops automatically upon completion. Save rehabilitation data and export assessment report. Remove electrodes, clean electrodes and contact area; power‑off and store equipment.
MyoNet‑COW supports Bluetooth connection to central workstation for data upload and multi‑case management.
Operation shall only be perｆormed by trained physicians or therapists in medical institutions.
6 适应症 Indications
中文采集体表肌电信号进行反馈训练，施加电刺激辅助治疗肌肉功能障碍；用于脑损伤所致肢体运动功能障碍、排尿功能障碍的康复训练；盆底肌肉功能障碍康复评估与训练，改善肌肉收缩、放松控制能力。
EnglishAcquire surface EMG signals for biofeedback training and apply electrical stimulation to assist therapy for muscular dysfunction. For rehabilitation training of limb motor dysfunction and micturition dysfunction caused by brain injury; rehabilitation assessment and training for pelvic‑floor muscular dysfunction to improve muscle contraction‑relaxation control.
7 禁忌症 Contraindications
中文
体内植入心脏起搏器、植入式除颤器患者；
治疗部位恶性肿瘤；
治疗部位皮肤破损、急性化脓感染、活动性出血；
严重认知障碍无法配合训练；
妊娠期间腹部、盆底腔内电极刺激；
癫痫发作期；
电极接触部位金属植入物（刺激输出通道）。
English
Patients with implanted cardiac pacemaker or implantable defibrillator.
Malignant tumor at treatment site.
Skin damage, acute pyogenic infection or active bleeding on target area.
Severe cognitive impairment unable to cooperate.
Abdominal or intracavitary pelvic‑floor stimulation during pregnancy.
Active epileptic seizure phase.
Metallic implants underneath stimulation electrode contact area.
8 注意事项 Precautions
中文
本设备为 Ⅱ 类医用康复设备，仅医疗机构内使用，禁止家用自行操作。
使用从最低刺激强度开始，缓慢上调，以患者可耐受无刺痛为准；严禁超耐受强度输出。
腔内电极必须严格消毒，避免交叉感染；电极破损严禁继续使用。
治疗过程中如出现疼痛、头晕、心慌等不适，立刻终止治疗。
不可将刺激电极置于颈动脉窦、头面部、胸口心脏区域。
定期校验设备，线缆、电极耗材按寿命更换。
不要在强电磁干扰环境下开展治疗。
治疗前确认无禁忌症，治疗全程治疗师监护。
English
Class Ⅱ medical rehabilitation device for institutional use only; no unsupervised home‑use permitted.
Start stimulation at minimal intensity and increase gradually to patient‑tolerable level without stabbing pain. Do not exceed patient tolerance.
Strictly disinfect intracavitary electrodes to avoid cross‑infection. Do not use damaged electrodes.
Immediately terminate therapy if pain, dizziness, palpitation or other adverse reactions occur.
Do not place stimulation electrodes over carotid sinus, head‑face or precardiac cardiac region.
Perｆorm periodic equipment calibration; replace cables and consumable electrodes according to service life.
Avoid therapy under strong electromagnetic interference.
Confirm no contraindications before treatment; therapist supervision is required during the whole session.
9 存储条件 Storage Conditions
中文环境温度：‑10℃～+40℃；相对湿度：30%‑80%，无凝露；大气压力：700hPa‑1060hPa；存放于干燥通风室内，避免阳光直射、粉尘、腐蚀性气体；设备断电存放；电极耗材按配件说明书条件保存国家药品监...。
EnglishAmbient temperature:‑10℃～+40℃; Relative humidity: 30%‑80%, non‑condensing; Atmospheric pressure:700hPa‑1060hPa. Store in dry and ventilated indoor area, avoid direct sunlight, dust and corrosive gas. Keep device powered‑off. Store electrode consumables in accordance with accessory manual国家药品监....
免责声明：以上产品详情仅供参考，临床操作请以原厂纸质说明书为准。上海康世达医疗器械有限公司不生产医疗产品，所有产品均来自产品的生产厂家，代理商，经销商，如有侵权请联系我们，会尽快处理！The above product details are for reference only. All clinical operations shall be carried out in strict accordance with the original paper instructions for use issued by the manufacturer.
Shanghai Kangshida Medical Devices Co., Ltd. does not manufacture medical devices. All products are sourced from respective manufacturers, authorized agents and distributors.
Please contact us promptly in case of any infringement, and we will resolve the matter as soon as possible.
热门标签：厂家直供诺诚肌电生物反馈仪MyoNet-COWMyoNet-BOW,诺诚肌电生物反馈仪,诺诚生物反馈仪
