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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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Thomas Select — 2 UDI-DI variants, MDR (Laerdal Medical AS)

MD Atlas
Laerdal Medical AS

Data from EUDAMED, last updated May 30, 2026

Thomas Select

0704543209935T3

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: Laerdal Medical AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0704543209935T3
Device name: Thomas Select
Device model: Thomas Select
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Laerdal Medical AS
SRN: NO-MF-000000012
Country: Norway
Email: PRRC@laerdal.com
Phone: +47 51511700

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GG6Z6F09R2RC4RAFKHBP7WPQ

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

600-4250007045432072310
600-4000007045432071870