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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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Activity chair — 15 UDI-DI variants, MDR (Schuchmann GmbH & Co. KG)

MD Atlas
Schuchmann GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Activity chair

4251040200004000720XXXXBB

15 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: Schuchmann GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4251040200004000720XXXXBB
Device name: Activity chair
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Schuchmann GmbH & Co. KG
SRN: DE-MF-000013435
Country: Germany
Email: info@schuchmann.de
Phone: +49 5402 407100

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01GFTSBPFQ1Q04MTNQS517QKF3

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

72 01 30004251040204644
72 02 20004251040204620
72 02 30004251040204651
72 01 10004251040204613
72 00 20004251040204606
72 00 30004251040204637
72 01 60004251040204736
72 02 60004251040204743
72 00 50004251040204699
72 02 40004251040204682
72 00 60004251040204729
72 01 40004251040204675
72 01 50004251040204705
72 02 50004251040204712
72 00 40004251040204668