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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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ODE SEATING SYSTEM — 12 UDI-DI variants, MDR (Timoteos Oy)

MD Atlas
Timoteos Oy

Data from EUDAMED, last updated May 23, 2026

ODE SEATING SYSTEM

643001637ODED5

12 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: 643001637ODED5
Device name: ODE SEATING SYSTEM
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

12 UDI-DI variants

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Applied filters

basicUdiUlid01FJVFND7V4ZE7PND152ESHFGD

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

ODE INDOOR BASE06430016370172
ODE INDOOR BASE06430016370134
ODE INDOOR BASE06430016370141
ODE INDOOR BASE06430016370189
ODE INDOOR BASE06430016370127
ODE OUTDOOR BASE06430016370196
ODE OUTDOOR BASE06430016370165
ODE OUTDOOR BASE06430016370202
ODE OUTDOOR BASE06430016370158
ODE SEAT06430016370110
ODE SEAT06430016370097
ODE SEAT06430016370103