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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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ELLA STANDER — 16 UDI-DI variants, MDR (Timoteos Oy)

MD Atlas
Timoteos Oy

Data from EUDAMED, last updated May 23, 2026

ELLA STANDER

643001637ELLA5U

16 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: Timoteos Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643001637ELLA5U
Device name: ELLA STANDER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 2021

Manufacturer & authorised representative

Manufacturer

Name: Timoteos Oy
SRN: FI-MF-000011749
Country: Finland
Email: timoteos@timoteos.fi

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01FJV54PQKN5FXRCH1QQJMCAKX

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

ELLA STANDER06430016370042
ELLA STANDER06430016370011
ELLA STANDER06430016370257
ELLA STANDER06430016370066
ELLA STANDER06430016370035
ELLA STANDER06430016370318
ELLA STANDER06430016370080
ELLA STANDER06430016370059
ELLA STANDER06430016370219
ELLA STANDER06430016370073
ELLA STANDER06430016370226
ELLA STANDER06430016370004
ELLA STANDER06430016370028
ELLA STANDER06430016370301
ELLA STANDER06430016370240
ELLA STANDER06430016370233