Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Liege - aktives Produkt — 71 UDI-DI variants, MDR (K.H. Dewert GmbH)

MD Atlas
K.H. Dewert GmbH

Data from EUDAMED, last updated May 23, 2026

Liege - aktives Produkt

4063907KHDewertELiegenE4

71 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4063907KHDewertELiegenE4
Device name: Liege - aktives Produkt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 28, 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

71 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KB5BZD7D2SXP9R1C8T0RXSYH

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

290040639070019964
4000E40639070014150
4001E40639070014228
4800E40639070016062
4802E40639070016130
4804E40639070016208
4815E40639070019032
4840E40639070019100
6000E40639070014396
6001E40639070014464
6050E40639070014532
6051E40639070014600
6070E40639070014778
6075E40639070014846
6080E40639070014914
6085E40639070015072
6100E40639070015140
7209E40639070015218
7255E40639070015386
90040639070019896
90E40639070002652

1 2 3