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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

Alvie — Class I MDR by Anker Health GmbH

MD Atlas
Anker Health GmbH

EUDAMED last updated this device on Jun 13, 2025

Alvie

426252606ALVIE65

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Anker Health GmbH
UDI-DI code: 04262526061118
Reference / catalog number: Alvie

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Manufacturer information

Organization name: Anker Health GmbH
SRN: DE-MF-000048131
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: not provided
UDI-DI code: 04262526061118
Basic UDI-DI: 426252606ALVIE65
Reference / catalog number: Alvie
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: Bei Alvie handelt es sich um eine Software zur patientenindividuellen Behandlung von unspezifischen Schmerzen im Bereich der Halswirbelsäule (HWS) sowie im Bereich der Brust- (BWS) und Lendenwirbelsäule (LWS). Durch die algorithmusgestützte Ausgabe patientenindividueller Trainings sowie die Bereitstellung von gesundheitsbezogenen Informationen und Entspannungsübungen werden der Rückenschmerz und die Lebensqualität der Nutzer:innen verbessert, sowie die Gesundheitskompetenz und Therapietreue (Adhärenz) erhöht.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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.