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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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Surgical Monitor — 6 UDI-DI variants, MDR (ADLINK Technology GmbH)

MD Atlas
ADLINK Technology GmbH

Data from EUDAMED, last updated May 23, 2026

Surgical Monitor

426065769ASM00000G5

6 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: 426065769ASM00000G5
Device name: Surgical Monitor
Device model: ASMXX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 4, 2024

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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJKMN877X8X35PSBVQNP7ZS5

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-DM32G-1004260657690337
93-DM24X-XXXX04260657690689
93-DM27X-XXXX04260657690696
93-DM3XX-XXXX04260657690702
93-DM31G-1004260657690320
93-DM43G-XXXX04260657690719