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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Orthopädisches Kopfkissen — 4 UDI-DI variants, MDR

MD Atlas
feela., Marco Winter, e-Commerce

Data from EUDAMED, last updated May 23, 2026

Orthopädisches Kopfkissen

4744999460720240X2D

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: feela., Marco Winter, e-Commerce

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4744999460720240X2D
Device name: Orthopädisches Kopfkissen
Device model: 202 401, 202 402, 202 403
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 14, 2024

Manufacturer & authorised representative

Manufacturer

Name: feela., Marco Winter, e-Commerce
SRN: DE-MF-000011263
Country: Germany
Email: info@feela.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JA5SHHC58XM0Q0SRV86DKVXW

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

202 401, 202 402, 202 40304744999460785
204 40304744999460815
202 40104744999460808
203 40204744999460792