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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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Orthopedic products — 17 UDI-DI variants, MDR (TONUS ELAST SIA)

MD Atlas
TONUS ELAST SIA

Data from EUDAMED, last updated May 31, 2026

Orthopedic products

4750283ELBOWVK

17 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: 4750283ELBOWVK
Device name: Orthopedic products
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 5, 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

17 UDI-DI variants

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Applied filters

basicUdiUlid01JWZBXJPJ4S6CM6WR5M8MQ626

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 960504750283006300
ELAST 960504750283006294
ELAST 960504750283006287
ELAST 960504750283006270
ELAST 021204750283040922
ELAST 021104750283041011
ELAST 0211 LUX04750283070233
ELAST 021204750283040960
ELAST 021204750283040946
ELAST 021204750283069343
ELAST 021104750283041004
ELAST 021204750283040939
ELAST 021104750283040977
ELAST 021204750283040953
ELAST 021104750283040991
ELAST 021104750283040984
ELAST 021104750283044340