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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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femSense — 6 UDI-DI variants, MDR (SteadySense GmbH)

MD Atlas
SteadySense GmbH

Data from EUDAMED, last updated May 23, 2026

femSense

912009590FEM012L

6 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: SteadySense GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 912009590FEM012L
Device name: femSense
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: SteadySense GmbH
SRN: AT-MF-000003984
Country: Austria
Email: office@steadysense.at
Phone: +43316232004

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GANFD9M2K13FNRNRG0E21EN4

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

femSense09120095900069
femSense09120095900052
femSense Fertility09120095900519
femSense Fertility09120095900502
femSense Fertility09120095900250
medicare femSense09120095900090