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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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Fertile Window — 4 UDI-DI variants, MDR (Oura Health Oy)

MD Atlas
Oura Health Oy

Data from EUDAMED, last updated May 23, 2026

Fertile Window

643006015Fertility72

4 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: Oura Health Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 643006015Fertility72
Device name: Fertile Window
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Sep 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Oura Health Oy
SRN: FI-MF-000037866
Country: Finland
Email: info@ouraring.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J8MQ8Y3BRYHVCQWDF15B36NM

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

Fertile Window06430060159877
Fertile Window06430060159860
Fertile Window06430060159990
Fertile Window06430060159983