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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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Organization name
UDI-DI code
Reference / catalog number

femSense Fertility — Class I MDR by SteadySense GmbH

MD Atlas
SteadySense GmbH

EUDAMED last updated this device on Jul 10, 2025

femSense Fertility

912009590FEM012L

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SteadySense GmbH
UDI-DI code: 09120095900502
Reference / catalog number: 09120095900502

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Manufacturer information

Organization name: SteadySense GmbH
SRN: AT-MF-000003984
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
Section Contraindications

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: femSense Fertility
UDI-DI code: 09120095900502
Basic UDI-DI: 912009590FEM012L
Reference / catalog number: 09120095900502
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 3
Additional product description: femSense Fertility is an information system intended for women in their fertile phase delivering information about the fertility status
Additional information URL: https://www.femsense.com/user-manual
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0399MEASUREMENT DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.