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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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HTS — 17 UDI-DI variants, MDR (Schuchmann GmbH & Co. KG)

MD Atlas
Schuchmann GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

HTS

4251040200004000570XXXXCA

17 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: 4251040200004000570XXXXCA
Device name: HTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 2, 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

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GNS24BAF1QJZFEKKW42H74KX

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

57 01 00004251040202800
57 02 00004251040202817
57 03 00004251040202824
Z16604251040203579
Z16704251040203586
Z16804251040203593
57 02 02504251040203418
57 02 00204251040203449
57 03 03004251040203500
57 03 00204251040203456
57 03 02504251040203425
57 01 03004251040203494
57 01 02504251040203401
57 01 00204251040203432
57 01 02604251040203463
57 01 00304251040203517
57 02 02604251040203470