Solawave (UDI PH-e03)
Manufactured by Shenzhen Goodwind technology development Co.,Ltd
Device Regulatory Overview
The Solawave (Model/Catalog Number: PH-e03) is a medical device manufactured by Shenzhen Goodwind technology development Co.,Ltd. This product is indexed under FDA Product Code / Category Classification ILY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PH-e03
- Product Code / EMDN
- ILY
- Device Name
- Solawave eye recovery pro
- Database Sync Date
- 2026-08-09 09:05:24
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 Solawave?
The registered manufacturer of record for Solawave is Shenzhen Goodwind technology development Co.,Ltd.
What is the Primary UDI-DI identifier for Solawave?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PH-e03.
What classification code is assigned to this device?
This device is registered under product classification code ILY.
Similar Classification Devices (ILY)
Other Devices by Shenzhen Goodwind technology development Co.,Ltd
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