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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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OvulaRing - Biosensor — 2 UDI-DI variants, MDR (VivoSensMedical GmbH)

MD Atlas
VivoSensMedical GmbH

Data from EUDAMED, last updated May 23, 2026

OvulaRing - Biosensor

426035994OVULT

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: VivoSensMedical GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426035994OVULT
Device name: OvulaRing - Biosensor
Device model: OVU-BS-2.4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: VivoSensMedical GmbH
SRN: DE-MF-000007273
Country: Germany
Email: info@vivosensmedical.com
Phone: +49 341 355 878 95

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQYC14DYE27ZWJ19HJ6S93K1

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

OVU-KR-204260359940129
OVU-BS-2.404260359940112