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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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Sascha — 6 UDI-DI variants, MDR (Schuchmann GmbH & Co. KG)

MD Atlas
Schuchmann GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Sascha

4251040200004000140XXXX8X

6 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: 4251040200004000140XXXX8X
Device name: Sascha
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01GG7H6R1CM9XW34A7YY6KF674

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

14 03 00104251040200646
14 01 10004251040200615
14 02 10004251040200639
14 02 00104251040200622
14 03 10004251040200653
14 01 00104251040200608