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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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Wave — 9 UDI-DI variants, MDR (Schuchmann GmbH & Co. KG)

MD Atlas
Schuchmann GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Wave

4251040200004000580XXXXCP

9 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: 4251040200004000580XXXXCP
Device name: Wave
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 5, 2023

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

9 UDI-DI variants

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Applied filters

basicUdiUlid01GP0TSEKTMJJGPANK3K669J7Q

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

58 01 10004251040202916
58 02 00004251040202923
58 01 00004251040202909
58 02 10004251040202930
58 03 00004251040202947
58 03 10004251040202954
58 00 51004251040203548
58 00 50004251040203531
58 00 52004251040203555