gudid
Primary ID: 09744428190
Elecsys HCG+ beta (UDI 09744428190)
Manufactured by Roche Diagnostics GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elecsys HCG+ beta - Primary ID 09744428190
Device Regulatory Overview
The Elecsys HCG+ beta (Model/Catalog Number: 09744428190) is a medical device manufactured by Roche Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification DHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09744428190
- Product Code / EMDN
- DHA
- Device Name
- Database Sync Date
- 2026-08-09 09:44:46
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 Elecsys HCG+ beta?
The registered manufacturer of record for Elecsys HCG+ beta is Roche Diagnostics GmbH.
What is the Primary UDI-DI identifier for Elecsys HCG+ beta?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09744428190.
What classification code is assigned to this device?
This device is registered under product classification code DHA.
Similar Classification Devices (DHA)
Other Devices by Roche Diagnostics GmbH
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