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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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Narcotrend Patient lead — 17 UDI-DI variants, MDR

MD Atlas
MT MonitorTechnik GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Narcotrend Patient lead

426049702Patientlead_PKK5

17 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: MT MonitorTechnik GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426049702Patientlead_PKK5
Device name: Narcotrend Patient lead
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: MT MonitorTechnik GmbH & Co. KG
SRN: DE-MF-000005317
Country: Germany
Email: info@monitortechnik.de

Variants by status

UDI-DI variants

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDT5854YB05AXRXBP4945WD

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

EK-031504260497025146
EK-030304260497025023
EK-030404260497025030
EK-030504260497025054
EK-031304260497025122
EK-031404260497025139
EK-030104260497025009
EK-031604260497025177
EK-030204260497025047
EK-030604260497025016
EK-031704260497025184
EK-031004260497025092
EK-031104260497025108
EK-031204260497025115
EK-030704260497025061
EK-030804260497025078
EK-030904260497025085