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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 Keilkissen — 10 UDI-DI variants, MDR

MD Atlas
feela., Marco Winter, e-Commerce

Data from EUDAMED, last updated May 23, 2026

Orthopädisches Keilkissen

47449994620220XZP

10 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: 47449994620220XZP
Device name: Orthopädisches Keilkissen
Device model: Art. 202 201, 202 202, 202 203
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 30, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01HNCH33QZJF1MGC0J4TDQ84TH

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

202 201, 202 202, 202 20304744999460754
202 201 - Silber04744999460372
202 201 - Dunkelgrau04744999460402
202 201 - Schwarz04744999460341
202 202 - Dunkelgrau04744999460396
202 202 - Schwarz04744999460334
202 202 - Silber04744999460365
202 203 - Dunkelgrau04744999460419
202 203 - Schwarz04744999460358
202 203 - Silber04744999460389