SANO (UDI SHE-MSP001)
Manufactured by Beijing Sano Lasers S&T Development Co., Ltd.
Device Regulatory Overview
The SANO (Model/Catalog Number: SHE-MSP001) is a medical device manufactured by Beijing Sano Lasers S&T Development Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NGX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SHE-MSP001
- Product Code / EMDN
- NGX
- Device Name
- The proposed device is a type of the most advanced electromagnetic,non-invasive treatment machine (with attachments). It is used for muscle tension enhancement and muscle strengthening on abdomen, hips, thighs, arms,etc.Three models (SHE-MSP003, SHE-MSP002 and SHE-MSP001) are included in HI-EMT MAGSHAPE series products, and they have thesame intended purposes, working theories and specifications.
- Database Sync Date
- 2026-08-09 09:06:39
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SANO?
The registered manufacturer of record for SANO is Beijing Sano Lasers S&T Development Co., Ltd..
What is the Primary UDI-DI identifier for SANO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SHE-MSP001.
What classification code is assigned to this device?
This device is registered under product classification code NGX.
Similar Classification Devices (NGX)
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