GUDIDData
eudamed_udi Primary ID: G07310102510

Therapiestuhl Nele Classic Gr.1 (UDI G07310102510)

Manufactured by Rehatec GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Therapiestuhl Nele Classic Gr.1 - Primary ID G07310102510

Device Regulatory Overview

The Therapiestuhl Nele Classic Gr.1 (Model/Catalog Number: 10102510) is a medical device manufactured by Rehatec GmbH. This product is indexed under FDA Product Code / Category Classification Y180980 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10102510
Product Code / EMDN
Y180980
Device Name
Therapiestuhl Nele
Database Sync Date
2026-08-09 16:51:44

Full Regulatory Attributes

πŸ”’ 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 Therapiestuhl Nele Classic Gr.1?

The registered manufacturer of record for Therapiestuhl Nele Classic Gr.1 is Rehatec GmbH.

What is the Primary UDI-DI identifier for Therapiestuhl Nele Classic Gr.1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G07310102510.

What classification code is assigned to this device?

This device is registered under product classification code Y180980.

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