gudid
Primary ID: 1230-003
QuPID Plus Sample Pack (UDI 1230-003)
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 Sample Pack - Primary ID 1230-003
Device Regulatory Overview
The QuPID Plus Sample Pack (Model/Catalog Number: 1230-003) 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
- 1230-003
- 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
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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 QuPID Plus Sample Pack?
The registered manufacturer of record for QuPID Plus Sample Pack is STANBIO LABORATORY, L.P..
What is the Primary UDI-DI identifier for QuPID Plus Sample Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1230-003.
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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