gudid
Primary ID: 3374
One+Step UTI (UDI 3374)
Manufactured by DFI CO.,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for One+Step UTI - Primary ID 3374
Device Regulatory Overview
The One+Step UTI (Model/Catalog Number: 3374) is a medical device manufactured by DFI CO.,LTD. This product is indexed under FDA Product Code / Category Classification LJX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3374
- Product Code / EMDN
- LJX
- Device Name
- The one device included 100 Strips
- Database Sync Date
- 2026-08-09 09:27:59
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 One+Step UTI?
The registered manufacturer of record for One+Step UTI is DFI CO.,LTD.
What is the Primary UDI-DI identifier for One+Step UTI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3374.
What classification code is assigned to this device?
This device is registered under product classification code LJX.
Similar Classification Devices (LJX)
Other Devices by DFI CO.,LTD
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