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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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KL 20 — 2 UDI-DI variants, MDR

MD Atlas
Achim Schulz-Lauterbach Vertrieb medizinischer Produkte GmbH

Data from EUDAMED, last updated May 23, 2026

KL 20

426077066kl20J9

2 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: Achim Schulz-Lauterbach Vertrieb medizinischer Produkte GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426077066kl20J9
Device name: KL 20
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: Achim Schulz-Lauterbach Vertrieb medizinischer Produkte GmbH
SRN: DE-MF-000018682
Country: Germany
Email: info@akut-dialyse.de
Phone: +492371/9763-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FZG1ZK18QF4ZJSW44YVV5RB9

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

KL 204260770660026
KL 204260770660002