gudid
Primary ID: W1-S10
Wondfo (UDI W1-S10)
Manufactured by WONDFO USA CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wondfo - Primary ID W1-S10
Device Regulatory Overview
The Wondfo (Model/Catalog Number: W1-S10) is a medical device manufactured by WONDFO USA CO., LTD.. This product is indexed under FDA Product Code / Category Classification JHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W1-S10
- Product Code / EMDN
- JHI
- Device Name
- 25-Strip; hCG Pregnancy Test 10mIU
- Database Sync Date
- 2026-08-09 09:31:26
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 Wondfo?
The registered manufacturer of record for Wondfo is WONDFO USA CO., LTD..
What is the Primary UDI-DI identifier for Wondfo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W1-S10.
What classification code is assigned to this device?
This device is registered under product classification code JHI.
Similar Classification Devices (JHI)
Other Devices by WONDFO USA CO., LTD.
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