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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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Medical elastic compression products — 199 UDI-DI variants, MDR

MD Atlas
TONUS ELAST SIA

Data from EUDAMED, last updated May 31, 2026

Medical elastic compression products

4750283CMLK2U2

199 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: TONUS ELAST SIA

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UDI-DI variants

199 UDI-DI variants

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Applied filters

basicUdiUlid01JVT4NTHZZ6Z9XG7JTACEAGTJ

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

ELAST 0401 LUX04750283026797
ELAST 0408 LUX04750283054462
ELAST 0401 Soft04750283077683
ELAST 0401 Soft04750283077706
ELAST 0401 Soft04750283077577
ELAST 0408 Soft04750283080263
ELAST 0401 Soft04750283077720
ELAST 0401 Soft04750283081437
ELAST 0408 Soft04750283081260
ELAST 0408 LUX04750283054516
ELAST 0401 LUX04750283026643
ELAST 0401 Soft04750283081475
ELAST 0408 Soft04750283080126
ELAST 0401 LUX04750283026858
ELAST 0408 Soft04750283080133
ELAST 0408 LUX04750283030909
ELAST 0408 Soft04750283080577
ELAST 0401 LUX04750283026810
ELAST 0401 Soft04750283081512
ELAST 0408 LUX04750283030763
ELAST 0401 LUX04750283026803
ELAST 0401 LUX04750283053946
ELAST 0401 Soft04750283077560
ELAST 0401 Soft04750283077690
ELAST 0408 LUX04750283054493

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4750283CMLK2U2
Device name: Medical elastic compression products
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: TONUS ELAST SIA
SRN: LV-MF-000006828
Country: Latvia
Email: info@tonuselast.com
Phone: +37120297040

Variants by status