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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 compression products — 96 UDI-DI variants, MDR

MD Atlas
TONUS ELAST SIA

Data from EUDAMED, last updated May 31, 2026

Medical compression products

4750283JZTS13B

96 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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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4750283JZTS13B
Device name: Medical compression products
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

96 UDI-DI variants

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Applied filters

basicUdiUlid01JVQGKREAARQSPT2G0VQJY7G6

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

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