eudamed_udi Primary ID: 08435025945449

CEINTURE LOMBOBELT RENFORT NOIR 24/H21 T5 (UDI 08435025945449)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CEINTURE LOMBOBELT RENFORT NOIR 24/H21 T5 (Model/Catalog Number: TR0238215) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y060308 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TR0238215
Product Code / EMDN: Y060308
Device Name: RACHIS LOMBAIRE
Database Sync Date: 2026-08-09 16:29:09

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 CEINTURE LOMBOBELT RENFORT NOIR 24/H21 T5?

The registered manufacturer of record for CEINTURE LOMBOBELT RENFORT NOIR 24/H21 T5 is Orliman, S.L.U..

What is the Primary UDI-DI identifier for CEINTURE LOMBOBELT RENFORT NOIR 24/H21 T5?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435025945449.

What classification code is assigned to this device?

This device is registered under product classification code Y060308.

Similar Classification Devices (Y060308)

Other Devices by Orliman, S.L.U.

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