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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

PI88445719 — Class I MDR by Powerinsole VertriebsgmbH

MD Atlas
Powerinsole VertriebsgmbH

EUDAMED last updated this device on Jan 13, 2026

PI88445719

912007566Pi20258Q

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Powerinsole VertriebsgmbH
UDI-DI code: 09120075660013
Reference / catalog number: PI88445719

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Manufacturer information

Organization name: Powerinsole VertriebsgmbH
SRN: AT-MF-000049851
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 09120075660013
Basic UDI-DI: 912007566Pi20258Q
Reference / catalog number: PI88445719
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: tragbares, nicht-invasives Medizinprodukt zur Unterstützung der Linderung chronischer Schmerzen des Bewegungsapparates (z. B. Rücken, Nacken, Schulter, Knie, Füße) mittels polymorphem Magnetfeld."
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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.