GUDIDData
eudamed_udi Primary ID: 00690650022585

Vertical Frame - SPX Max Plus (Jet Black) (UDI 00690650022585)

Manufactured by Merrithew International Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vertical Frame - SPX Max Plus (Jet Black) - Primary ID 00690650022585

Device Regulatory Overview

The Vertical Frame - SPX Max Plus (Jet Black) (Model/Catalog Number: ST-02258) is a medical device manufactured by Merrithew International Inc. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ST-02258
Product Code / EMDN
Z12069099
Device Name
VERTICAL FRAME
Database Sync Date
2026-08-09 16:29:01

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 Vertical Frame - SPX Max Plus (Jet Black)?

The registered manufacturer of record for Vertical Frame - SPX Max Plus (Jet Black) is Merrithew International Inc.

What is the Primary UDI-DI identifier for Vertical Frame - SPX Max Plus (Jet Black)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00690650022585.

What classification code is assigned to this device?

This device is registered under product classification code Z12069099.

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