GUDIDData
eudamed_udi Primary ID: G07310240580

Therapiestuhl Pauli Gr.2 (UDI G07310240580)

Manufactured by Rehatec GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Therapiestuhl Pauli Gr.2 - Primary ID G07310240580

Device Regulatory Overview

The Therapiestuhl Pauli Gr.2 (Model/Catalog Number: 1024058) 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
1024058
Product Code / EMDN
Y180980
Device Name
Therapiestuhl Nele
Database Sync Date
2026-08-09 17:48:54

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 Pauli Gr.2?

The registered manufacturer of record for Therapiestuhl Pauli Gr.2 is Rehatec GmbH.

What is the Primary UDI-DI identifier for Therapiestuhl Pauli Gr.2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G07310240580.

What classification code is assigned to this device?

This device is registered under product classification code Y180980.

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