GUDIDData
gudid Primary ID: JC35M3-L

maideiste (UDI JC35M3-L)

Manufactured by Hangzhou Guoyuan Yanglao Technology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for maideiste - Primary ID JC35M3-L

Device Regulatory Overview

The maideiste (Model/Catalog Number: JC35M3-L) is a medical device manufactured by Hangzhou Guoyuan Yanglao Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification FRZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
JC35M3-L
Product Code / EMDN
FRZ
Device Name
Database Sync Date
2026-08-09 09:18:23

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 maideiste?

The registered manufacturer of record for maideiste is Hangzhou Guoyuan Yanglao Technology Co., Ltd.

What is the Primary UDI-DI identifier for maideiste?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is JC35M3-L.

What classification code is assigned to this device?

This device is registered under product classification code FRZ.

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