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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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Liegen - Nicht aktives Produkt — 87 UDI-DI variants, MDR

MD Atlas
K.H. Dewert GmbH

Data from EUDAMED, last updated May 23, 2026

Liegen - Nicht aktives Produkt

4063907KHDewertLiegenP2

87 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: K.H. Dewert GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4063907KHDewertLiegenP2
Device name: Liegen - Nicht aktives Produkt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: K.H. Dewert GmbH
SRN: DE-MF-000005967
Country: Germany
Email: info@khdewert.de

Variants by status

UDI-DI variants

87 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBQFHG37602Q3J7NHBZDWH6S

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

2880XL/H40639070018288
2890XL/H40639070018660
2895XL/H40639070018806
3040639070020540
3140639070020090
3240639070002034
3640639070002102
3740639070002270
6040639070020618
6140639070020304
7040639070020854
7140639070020786

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