GUDIDData
eudamed_udi Primary ID: 06972727560096

VertiPlatform (UDI 06972727560096)

Manufactured by Shanghai ZEHNIT Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VertiPlatform - Primary ID 06972727560096

Device Regulatory Overview

The VertiPlatform (Model/Catalog Number: 009) is a medical device manufactured by Shanghai ZEHNIT Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12062402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
009
Product Code / EMDN
Z12062402
Device Name
Balance Rehabilitation System
Database Sync Date
2026-08-09 16:46:02

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 VertiPlatform?

The registered manufacturer of record for VertiPlatform is Shanghai ZEHNIT Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for VertiPlatform?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972727560096.

What classification code is assigned to this device?

This device is registered under product classification code Z12062402.

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