GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 06977346241050

Unspecified Brand (UDI 06977346241050)

Manufactured by YIWU EASON MEDICAL DEVICES CO.,LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06977346241050

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 10mlÎŚ16*100pp) is a medical device manufactured by YIWU EASON MEDICAL DEVICES CO.,LTD.. This product is indexed under FDA Product Code / Category Classification W0599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10mlÎŚ16*100pp
Product Code / EMDN
W0599
Device Name
Test Tube
Database Sync Date
2026-08-09 16:28:44

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is YIWU EASON MEDICAL DEVICES CO.,LTD..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977346241050.

What classification code is assigned to this device?

This device is registered under product classification code W0599.

Similar Classification Devices (W0599)

Other Devices by YIWU EASON MEDICAL DEVICES CO.,LTD.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint