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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

ViViRA Knee — Class I MDR by Vivira Health Lab GmbH

MD Atlas
Vivira Health Lab GmbH

EUDAMED last updated this device on Oct 15, 2025

ViViRA Knee

426235644ViViRAKneeXT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vivira Health Lab GmbH
UDI-DI code: 04262356440923
Reference / catalog number: ViViRA Knie iOS

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Manufacturer information

Organization name: Vivira Health Lab GmbH
SRN: DE-MF-000006530
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: ViViRA Knee
UDI-DI code: 04262356440923
Basic UDI-DI: 426235644ViViRAKneeXT
Reference / catalog number: ViViRA Knie iOS
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: 1
Additional product description: ViViRA Knie ist ein therapeutisches Trainingsprogramm bei Knieschmerzen. Es richtet sich an Anwender mit Gonarthrose (Arthrose des Kniegelenks) und zielt darauf ab, muskuloskelettale Schmerzen aufgrund dieser Erkrankung zu reduzieren.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12069092VARIOUS PHYSIOTHERAPY AND REHABILITATION 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.