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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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MLC-S — 2 UDI-DI variants, MDR (ADLINK Technology GmbH)

MD Atlas
ADLINK Technology GmbH

Data from EUDAMED, last updated May 23, 2026

MLC-S

426065769MLCS0000T6

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: ADLINK Technology GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426065769MLCS0000T6
Device name: MLC-S
Device model: MLC-SXX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: ADLINK Technology GmbH
SRN: DE-MF-000012782
Country: Germany
Email: germany@adlinktech.com
Phone: +49 991 29094 10

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JA4ZDQT6QDBBEWC3E5DCR73R

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

93-D2103-XXXX04260657690726
93-D2303-XXXX04260657690733