gudid
Primary ID: 1230-050
QuPID Plus hCG (UDI 1230-050)
Manufactured by STANBIO LABORATORY, L.P.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QuPID Plus hCG - Primary ID 1230-050
Device Regulatory Overview
The QuPID Plus hCG (Model/Catalog Number: 1230-050) is a medical device manufactured by STANBIO LABORATORY, L.P.. This product is indexed under FDA Product Code / Category Classification JHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1230-050
- Product Code / EMDN
- JHI
- Device Name
- For the qualitative determination of human chorionic gonadotropin (hCG) in serum or urine to aid in the early detection of pregnancy.
- Database Sync Date
- 2026-08-09 09:17:29
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 QuPID Plus hCG?
The registered manufacturer of record for QuPID Plus hCG is STANBIO LABORATORY, L.P..
What is the Primary UDI-DI identifier for QuPID Plus hCG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1230-050.
What classification code is assigned to this device?
This device is registered under product classification code JHI.
Similar Classification Devices (JHI)
Other Devices by STANBIO LABORATORY, L.P.
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