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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

QoLibri — Class I MDR by NOVESIA

MD Atlas
NOVESIA

EUDAMED last updated this device on Nov 3, 2025

QoLibri

377003444SWNOVFP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NOVESIA
UDI-DI code: 03770034448006
Reference / catalog number: QoLibri

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Manufacturer information

Organization name: NOVESIA
SRN: FR-MF-000040879
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: QoLibri
UDI-DI code: 03770034448006
Basic UDI-DI: 377003444SWNOVFP
Reference / catalog number: QoLibri
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: QoLibri is a standalone Software as a Medical Device. It is a digital therapeutic solution intended for adults living with chronic pain. The software supports self-management strategies aimed at reducing functional impairment and enhancing patients' quality of life.
Additional information URL: https://novesia.fr/docs/QOL-manuel_utilisateur_patient.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12062492BIOFEEDBACK 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

Related devices

This device is not currently linked to any other device.

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.