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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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Oviva App — 2 UDI-DI variants, MDR (Oviva AG)

MD Atlas
Oviva AG

Data from EUDAMED, last updated May 23, 2026

Oviva App

7649993906NUTTH

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: Oviva AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7649993906NUTTH
Device name: Oviva App
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Oviva AG
SRN: CH-MF-000019928
Country: Switzerland
Email: kontakt@oviva.ch

Authorised representative

Name: Medical Technology Promedt Consulting GmbH
SRN: DE-AR-000000085
Country: Germany
Phone: +49 6894 581020

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KKKQ7C6H0CFTJ2BX9SE0FXJN

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

Oviva Direkt App iOS07649993906024
Oviva Direkt App Android07649993906048