GUDIDData
eudamed_udi Primary ID: 08806125680040

URiSCAN® 4 HemoGPH strip (UDI 08806125680040)

Manufactured by YD Diagnostics CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URiSCAN® 4 HemoGPH strip - Primary ID 08806125680040

Device Regulatory Overview

The URiSCAN® 4 HemoGPH strip (Model/Catalog Number: U12) is a medical device manufactured by YD Diagnostics CORP.. This product is indexed under FDA Product Code / Category Classification W0101060204,W0101060205 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
U12
Product Code / EMDN
W0101060204,W0101060205
Device Name
URiSCAN® strip (Professional use)
Database Sync Date
2026-08-09 16:30:37

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of URiSCAN® 4 HemoGPH strip?

The registered manufacturer of record for URiSCAN® 4 HemoGPH strip is YD Diagnostics CORP..

What is the Primary UDI-DI identifier for URiSCAN® 4 HemoGPH strip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806125680040.

What classification code is assigned to this device?

This device is registered under product classification code W0101060204,W0101060205.

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