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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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Ultraschall Bezug — 20 UDI-DI variants, MDR

MD Atlas
Udo Heisig GmbH The Disposables Company

Data from EUDAMED, last updated May 23, 2026

Ultraschall Bezug

42518062001KW

20 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: Udo Heisig GmbH The Disposables Company

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518062001KW
Device name: Ultraschall Bezug
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Udo Heisig GmbH The Disposables Company
SRN: DE-MF-000009334
Country: Germany
Email: info@heisig.de
Phone: 0894623920

Variants by status

UDI-DI variants

20 UDI-DI variants

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Applied filters

basicUdiUlid01FTTM1K7772H1J4HSQPPDE6ZZ

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

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3180004251806202730
3190004251806202679
3182504251806200521
3191204251806200606
3180304251806200439
3180504251806200453
3190804251806200583
3181204251806200507
3180804251806200477
3190304251806200545
3190504251806200569
3192504251806200620
3101104251806200293
3102004251806200316
3101604251806203249
3120004251806200330
3101504251806200309
3101304251806203294
3110004251806203218