GUDIDData
eudamed_udi Primary ID: G07310177070

Heidelberger Stehgerät Standard Gr.2 (UDI G07310177070)

Manufactured by Rehatec GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Heidelberger Stehgerät Standard Gr.2 - Primary ID G07310177070

Device Regulatory Overview

The Heidelberger Stehgerät Standard Gr.2 (Model/Catalog Number: 1017707) is a medical device manufactured by Rehatec GmbH. This product is indexed under FDA Product Code / Category Classification Y180939 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1017707
Product Code / EMDN
Y180939
Device Name
Heidelberger Liegebär Lasse
Database Sync Date
2026-08-09 16:30:17

Full Regulatory Attributes

🔒 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 Heidelberger Stehgerät Standard Gr.2?

The registered manufacturer of record for Heidelberger Stehgerät Standard Gr.2 is Rehatec GmbH.

What is the Primary UDI-DI identifier for Heidelberger Stehgerät Standard Gr.2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G07310177070.

What classification code is assigned to this device?

This device is registered under product classification code Y180939.

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