GUDIDData
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eudamed_udi Primary ID: 09420082902251

Spex (UDI 09420082902251)

Manufactured by Spex Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spex - Primary ID 09420082902251

Device Regulatory Overview

The Spex (Model/Catalog Number: 1257-1620-3FK_030) is a medical device manufactured by Spex Ltd. This product is indexed under FDA Product Code / Category Classification Y122406 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1257-1620-3FK_030
Product Code / EMDN
Y122406
Device Name
Wheelchair Back Support
Database Sync Date
2026-08-09 16:28:52

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 Spex?

The registered manufacturer of record for Spex is Spex Ltd.

What is the Primary UDI-DI identifier for Spex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09420082902251.

What classification code is assigned to this device?

This device is registered under product classification code Y122406.

Similar Classification Devices (Y122406)

Other Devices by Spex Ltd

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