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Organization name
UDI-DI code
Reference / catalog number

30207 — Class I MDR by INOS GmbH

MD Atlas
INOS GmbH

EUDAMED last updated this device on May 19, 2026

30207

PP09338FERSOMEDDRUCK09

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: INOS GmbH
UDI-DI code: 111714981276
Reference / catalog number: 30207

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Manufacturer information

Organization name: INOS GmbH
SRN: DE-MF-000044031
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Die FERSOmed® Druckstimulation darf bei folgenden Kontraindikationen nicht verwendet werden: Erkrankungen des Knochens wie Frakturen, Periostitis neurologische Erkrankungen wie Polyneuropathie, z. B. diabetische Polyneuropathie, Tarsal-Tunnel-Syndrom peripheren Durchblutungsstörungen (pAVK) oder Erkrankungen der Venen des betroffenen Beines Erkrankungen der Weichteile wie Bursitis oder ausgeprägtes Beinödem Infektionen und Verletzungen

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: 111714981276
Basic UDI-DI: PP09338FERSOMEDDRUCK09
Reference / catalog number: 30207
Issuing entity: IFA

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: Nur für Erwachsene. Die FERSOmed® Druckstimulation wird eingesetzt zur Behandlung von Beschwerden bei folgenden Indikationen: Plantarer Fersensporn (Dornartige Verknöcherung am unteren Fersenbein) Plantarfasziitis (Entzündung der Sehnenplatte) Insertionstendopathie der Plantarfaszie (Reizung des Sehnenansatzes an der Ferse)
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.