gudid
Primary ID: 30D4
One+Step 10A (UDI 30D4)
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 10A - Primary ID 30D4
Device Regulatory Overview
The One+Step 10A (Model/Catalog Number: 30D4) 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
- 30D4
- Product Code / EMDN
- LJX
- Device Name
- One device is included 100 test 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 10A?
The registered manufacturer of record for One+Step 10A is DFI CO.,LTD.
What is the Primary UDI-DI identifier for One+Step 10A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30D4.
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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