GUDIDData
eudamed_udi Primary ID: 04744999460136

Orthopädisches Sitzkissen - Art. 201 802 - Schwarz (UDI 04744999460136)

Manufactured by feela., Marco Winter, e-Commerce

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Orthopädisches Sitzkissen - Art. 201 802 - Schwarz - Primary ID 04744999460136

Device Regulatory Overview

The Orthopädisches Sitzkissen - Art. 201 802 - Schwarz (Model/Catalog Number: 201 802 - Schwarz) is a medical device manufactured by feela., Marco Winter, e-Commerce. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
201 802 - Schwarz
Product Code / EMDN
V08030102
Device Name
Orthopädisches Sitzkissen
Database Sync Date
2026-08-09 16:46:11

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 Orthopädisches Sitzkissen - Art. 201 802 - Schwarz?

The registered manufacturer of record for Orthopädisches Sitzkissen - Art. 201 802 - Schwarz is feela., Marco Winter, e-Commerce.

What is the Primary UDI-DI identifier for Orthopädisches Sitzkissen - Art. 201 802 - Schwarz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04744999460136.

What classification code is assigned to this device?

This device is registered under product classification code V08030102.

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