eudamed_udi
Primary ID: 17090041920535
Seronorm® HbA1c Liquid L-1 (UDI 17090041920535)
Manufactured by SERO AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Seronorm® HbA1c Liquid L-1 - Primary ID 17090041920535
Device Regulatory Overview
The Seronorm® HbA1c Liquid L-1 (Model/Catalog Number: 209005) is a medical device manufactured by SERO AS. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 209005
- Product Code / EMDN
- W0101050205
- Device Name
- Seronorm® HbA1c Liquid L-1
- Database Sync Date
- 2026-08-09 16:50:34
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 Seronorm® HbA1c Liquid L-1?
The registered manufacturer of record for Seronorm® HbA1c Liquid L-1 is SERO AS.
What is the Primary UDI-DI identifier for Seronorm® HbA1c Liquid L-1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 17090041920535.
What classification code is assigned to this device?
This device is registered under product classification code W0101050205.
Similar Classification Devices (W0101050205)
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