gudid
Primary ID: HCG-PRE-OTC10
Preview (UDI HCG-PRE-OTC10)
Manufactured by WONDFO USA CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Preview - Primary ID HCG-PRE-OTC10
Device Regulatory Overview
The Preview (Model/Catalog Number: HCG-PRE-OTC10) 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
- HCG-PRE-OTC10
- Product Code / EMDN
- JHI
- Device Name
- 1-Midstreams; hCG Pregnancy Midstream Test Retail Box 1 Pcs Preview 10 MIU
- Database Sync Date
- 2026-08-09 09:31:26
Full Regulatory Attributes
🔒 Token Gated
{
"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 Preview?
The registered manufacturer of record for Preview is WONDFO USA CO., LTD..
What is the Primary UDI-DI identifier for Preview?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HCG-PRE-OTC10.
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.
Programmatic Export
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