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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

Fr — Class I MDR by Lifeness A/S

MD Atlas
Lifeness A/S

EUDAMED last updated this device on May 21, 2025

Fr

709006306Wellapy630HB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lifeness A/S
UDI-DI code: 17090063060042
Reference / catalog number: Fr

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View device family (Basic UDI)

Manufacturer information

Organization name: Lifeness A/S
SRN: NO-MF-000047862
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Aug 31, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 17090063060042
Basic UDI-DI: 709006306Wellapy630HB
Reference / catalog number: Fr
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: A digital therapeutics application that treats obesity and related conditions through personalized nutrition, exercise, and behavioral therapy programs
Additional information URL: https://lifeness-no.notion.site/Wellapy-Mode-d-emploi-1eb97679e3b38136bb9ccb4d54d9fcb6?pvs=4
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)17090063060042

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q0399ENT DEVICES - OTHER
G030699DEVICES FOR THE NON-SURGICAL TREATMENT OF OBESITY - OTHER
Z12040292GENERAL MEDICINE THERAPEUTIC 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

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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.