gudid Primary ID: 2260

Blueline (UDI 2260)

Manufactured by Transparent Supply Solutions Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Blueline (Model/Catalog Number: 2260) is a medical device manufactured by Transparent Supply Solutions Ltd.. This product is indexed under FDA Product Code / Category Classification FXP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2260
Product Code / EMDN: FXP
Device Name: Shoe Cover, Non Skid, SPP, Blue, Universal
Database Sync Date: 2026-08-09 09:20:17

Full Regulatory Attributes

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{
    "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 Blueline?

The registered manufacturer of record for Blueline is Transparent Supply Solutions Ltd..

What is the Primary UDI-DI identifier for Blueline?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2260.

What classification code is assigned to this device?

This device is registered under product classification code FXP.

Similar Classification Devices (FXP)

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