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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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MR Introducer — 3 UDI-DI variants, MDR

MD Atlas
Clinical Laserthermia Systems AB

Data from EUDAMED, last updated May 30, 2026

MR Introducer

17340000005FD

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Clinical Laserthermia Systems AB

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 17340000005FD
Device name: MR Introducer
Device model: 4013-14
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Clinical Laserthermia Systems AB
SRN: SE-MF-000016898
Country: Sweden
Email: info@clinicallaser.se
Phone: +46 46152100

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JV4B9SFY1T98F2XCRAWGAGYP

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

Tranberg MR Introducer17340007000765
TRANBERG MR Introducer17340007000772
TRANBERG MR Introducer17340007000789