GUDIDData
eudamed_udi Primary ID: 04068429046852

Durchgehendes Seitengitter Holz 2183mm Königsahorn (UDI 04068429046852)

Manufactured by tecfor care GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Durchgehendes Seitengitter Holz 2183mm Königsahorn - Primary ID 04068429046852

Device Regulatory Overview

The Durchgehendes Seitengitter Holz 2183mm Königsahorn (Model/Catalog Number: 04685) is a medical device manufactured by tecfor care GmbH. This product is indexed under FDA Product Code / Category Classification V08068001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
04685
Product Code / EMDN
V08068001
Device Name
Seitengitter
Database Sync Date
2026-08-09 16:51:41

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 Durchgehendes Seitengitter Holz 2183mm Königsahorn?

The registered manufacturer of record for Durchgehendes Seitengitter Holz 2183mm Königsahorn is tecfor care GmbH.

What is the Primary UDI-DI identifier for Durchgehendes Seitengitter Holz 2183mm Königsahorn?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04068429046852.

What classification code is assigned to this device?

This device is registered under product classification code V08068001.

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