GUDIDData
eudamed_udi Primary ID: 06009880396184

STIMPOD ST2-3000 (UDI 06009880396184)

Manufactured by Xavant Technology (Pty) Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STIMPOD ST2-3000 - Primary ID 06009880396184

Device Regulatory Overview

The STIMPOD ST2-3000 (Model/Catalog Number: ST2-3000) is a medical device manufactured by Xavant Technology (Pty) Ltd. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ST2-3000
Product Code / EMDN
Z12062899
Device Name
Precision Nerve Locator
Database Sync Date
2026-08-09 17:50:49

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 STIMPOD ST2-3000?

The registered manufacturer of record for STIMPOD ST2-3000 is Xavant Technology (Pty) Ltd.

What is the Primary UDI-DI identifier for STIMPOD ST2-3000?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06009880396184.

What classification code is assigned to this device?

This device is registered under product classification code Z12062899.

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