gudid
Primary ID: 31H0P
One+Step Uric Acid (UDI 31H0P)
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 Uric Acid - Primary ID 31H0P
Device Regulatory Overview
The One+Step Uric Acid (Model/Catalog Number: 31H0P) is a medical device manufactured by DFI CO.,LTD. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31H0P
- Product Code / EMDN
- KNK
- Device Name
- 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 Uric Acid?
The registered manufacturer of record for One+Step Uric Acid is DFI CO.,LTD.
What is the Primary UDI-DI identifier for One+Step Uric Acid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31H0P.
What classification code is assigned to this device?
This device is registered under product classification code KNK.
Similar Classification Devices (KNK)
Other Devices by DFI CO.,LTD
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