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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

OVU-SW 5.x.x — Class I MDD by VivoSensMedical GmbH

MD Atlas
VivoSensMedical GmbH

EUDAMED last updated this device on May 20, 2026

OVU-SW 5.x.x

B-04260359940136

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VivoSensMedical GmbH
UDI-DI code: 04260359940136
Reference / catalog number: OVU-SW 5.x.x

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Manufacturer information

Organization name: VivoSensMedical GmbH
SRN: DE-MF-000007273
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2013	May 20, 2026

Device identification

Trade name: not provided
UDI-DI code: 04260359940136
Basic UDI-DI: B-04260359940136
Reference / catalog number: OVU-SW 5.x.x
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: SOFTWAREOvulaRing Software dient der softwaregestützten Analyse zur Fruchtbarkeitsüberwachung, Unterstützung bei Kinderwunsch und für Methoden der natürlichen Familienplanung. Der Intended Purpose liegt im Bereich Gynäkologie und Fertilitätsbehandlung.
Additional information URL: https://myovularing.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080292GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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

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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.