gudid
Primary ID: M-282
NOOANCE (UDI M-282)
Manufactured by Shenzhen Kaiyan Medical Equipment Co,. Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOOANCE - Primary ID M-282
Device Regulatory Overview
The NOOANCE (Model/Catalog Number: M-282) is a medical device manufactured by Shenzhen Kaiyan Medical Equipment Co,. Ltd. This product is indexed under FDA Product Code / Category Classification OAP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M-282
- Product Code / EMDN
- OAP
- Device Name
- The NOOANCE LED AND LASER HELME'T is indicated to promote hair growth in males with androgenetic alopeciawho have HamiltonNorwood Classifications of lla-V and Fitzpatrick Classification of Skin Phototypes I to IV, andfemales with androgenetic alopecia who have Ludwig-Savin Classifications of-ll and Fitzpatrick Classification of SkinPhototypes I to IV.
- Database Sync Date
- 2026-08-09 09:05:22
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 NOOANCE?
The registered manufacturer of record for NOOANCE is Shenzhen Kaiyan Medical Equipment Co,. Ltd.
What is the Primary UDI-DI identifier for NOOANCE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M-282.
What classification code is assigned to this device?
This device is registered under product classification code OAP.
Similar Classification Devices (OAP)
Other Devices by Shenzhen Kaiyan Medical Equipment Co,. Ltd
Programmatic Export
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