eudamed_udi
Primary ID: 03610230008393
Yumizen G IMIDAZOL (UDI 03610230008393)
Manufactured by HORIBA ABX SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Yumizen G IMIDAZOL - Primary ID 03610230008393
Device Regulatory Overview
The Yumizen G IMIDAZOL (Model/Catalog Number: 1300036385) is a medical device manufactured by HORIBA ABX SAS. This product is indexed under FDA Product Code / Category Classification W0103020999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1300036385
- Product Code / EMDN
- W0103020999
- Device Name
- Yumizen G IMIDAZOL
- Database Sync Date
- 2026-08-09 16:29:02
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 Yumizen G IMIDAZOL?
The registered manufacturer of record for Yumizen G IMIDAZOL is HORIBA ABX SAS.
What is the Primary UDI-DI identifier for Yumizen G IMIDAZOL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03610230008393.
What classification code is assigned to this device?
This device is registered under product classification code W0103020999.
Similar Classification Devices (W0103020999)
Other Devices by HORIBA ABX SAS
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