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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

9105212 — Class I MDR by WWS Ideen aus PU GmbH

MD Atlas
WWS Ideen aus PU GmbH

EUDAMED last updated this device on Mar 4, 2025

9105212

4262487769105BVW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: WWS Ideen aus PU GmbH
UDI-DI code: 04262487760143
Reference / catalog number: 9105212

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Manufacturer information

Organization name: WWS Ideen aus PU GmbH
SRN: DE-MF-000043534
Manufacturer status: Active

Related devices

91052094262487769105BVWOn the market 91052134262487769105BVWOn the market 91050174262487769105BVWOn the market 91052044262487769105BVWOn the market 91052114262487769105BVWOn the market

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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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: 04262487760143
Basic UDI-DI: 4262487769105BVW
Reference / catalog number: 9105212
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: M

EMDN nomenclature code(s)

Y061209KNEE ORTHOSES

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

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Expiration date
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Software identification