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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

45570 — Class I MDR by Künzli SwissSchuh AG

MD Atlas
Künzli SwissSchuh AG

EUDAMED last updated this device on Jul 25, 2025

45570

76300428Stabilschuhe5M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Künzli SwissSchuh AG
UDI-DI code: 07630042807287
Reference / catalog number: 45570

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Manufacturer information

Organization name: Künzli SwissSchuh AG
SRN: CH-MF-000044954
Manufacturer status: Active

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Critical warnings

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

CW010
Gebrauchsanweisung beachten und die Anweisungen des Arztes befolgen

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: 07630042807287
Basic UDI-DI: 76300428Stabilschuhe5M
Reference / catalog number: 45570
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: Der Künzli Ortho® Stabilschuh mit schmalem, femininem Schnitt stabilisiert Fuss und Sprunggelenk und ermöglicht eine frühfunktionelle Mobilisation nach Verletzungen oder bei Gangunsicherheit. Der hohe Schaft mit herausnehmbaren, thermoverformbaren Stabilisatoren sorgt für gezielte Unterstützung und sicheren Halt. Ein elastisches Vorfussband, Fersenriemen und Schnürung mit Haken und Ösen ermöglichen eine individuelle Anpassung. Der Schuh ist orthopädisch zurichtbar und für den täglichen Einsatz konzipiert.
Additional information URL: https://www.kuenzli-schuhe.ch/ortho_standardschuhe/Ortho-Donna-45570
Clinical sizes: 8 MU999

EMDN nomenclature code(s)

Y063303READY-MADE ORTHOTIC SHOES

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

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.