eudamed_udi
Primary ID: 06942202228612
DIRUI (UDI 06942202228612)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIRUI - Primary ID 06942202228612
Device Regulatory Overview
The DIRUI (Model/Catalog Number: Level 1:3×1mL) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Level 1:3×1mL
- Product Code / EMDN
- W0102152003
- Device Name
- Specific Protein Control
- Database Sync Date
- 2026-08-09 16:51:04
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 DIRUI?
The registered manufacturer of record for DIRUI is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for DIRUI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202228612.
What classification code is assigned to this device?
This device is registered under product classification code W0102152003.
Similar Classification Devices (W0102152003)
Other Devices by DIRUI INDUSTRIAL CO., LTD
Programmatic Export
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