Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Medical elastic compression products — 275 UDI-DI variants, MDR

MD Atlas
TONUS ELAST SIA

Data from EUDAMED, last updated May 31, 2026

Medical elastic compression products

4750283CMLB2T7

275 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4750283CMLB2T7
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 4, 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

275 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01JTE20B9HQNZMV15MCACJN8Z3

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

0402 LUX 2.004750283083646
0402 LUX 2.004750283083950
0403 LUX 2.004750283084360
0403 LUX 2.004750283084285
0402 LUX 2.004750283083684
0402 LUX 2.004750283083899
0402 LUX 2.004750283083936
0402 LUX 2.004750283083691
0402 LUX 2.004750283083615
0403 LUX 2.004750283084346
0403 LUX 2.004750283084148
0402 LUX 2.004750283083745
0403 LUX 2.004750283084353
0402 LUX 2.004750283083912
0403 LUX 2.004750283084162
0403 LUX 2.004750283084131
0403 LUX 2.004750283084315
0402 LUX 2.004750283083752
0402 LUX 2.004750283083608
0402 LUX 2.004750283083929
0403 LUX 2.004750283084094
0403 LUX 2.004750283084155
0403 LUX 2.004750283084100
0403 LUX 2.004750283084117
0403 LUX 2.004750283084087

1 2 3 4 5