GUDIDData
eudamed_udi Primary ID: 08806125621142

EASYPREP Gradient Density Reagent (UDI 08806125621142)

Manufactured by YD Diagnostics CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EASYPREP Gradient Density Reagent - Primary ID 08806125621142

Device Regulatory Overview

The EASYPREP Gradient Density Reagent (Model/Catalog Number: EZ 02) is a medical device manufactured by YD Diagnostics CORP.. This product is indexed under FDA Product Code / Category Classification W0202059085 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EZ 02
Product Code / EMDN
W0202059085
Device Name
EASYPREP kits
Database Sync Date
2026-08-09 17:34:51

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 EASYPREP Gradient Density Reagent?

The registered manufacturer of record for EASYPREP Gradient Density Reagent is YD Diagnostics CORP..

What is the Primary UDI-DI identifier for EASYPREP Gradient Density Reagent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806125621142.

What classification code is assigned to this device?

This device is registered under product classification code W0202059085.

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