gudid Primary ID: 7702

Blueline (UDI 7702)

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: 7702) is a medical device manufactured by Transparent Supply Solutions Ltd.. This product is indexed under FDA Product Code / Category Classification IPR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7702
Product Code / EMDN: IPR
Device Name: Aluminum Pair Crutch, Push Button Adjustable, Youth
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 7702.

What classification code is assigned to this device?

This device is registered under product classification code IPR.

Similar Classification Devices (IPR)

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