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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

WorkPark WP 1 Work shelf — Class I MDD by Nitzbon AG

MD Atlas
Nitzbon AG

EUDAMED last updated this device on May 26, 2026

WorkPark WP 1 Work shelf

B-04260101482006

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Nitzbon AG
UDI-DI code: 04260101482006
Reference / catalog number: 1621510

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Manufacturer information

Organization name: Nitzbon AG
SRN: DE-MF-000009971
Manufacturer status: Active

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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 2, 2014	Still on market

Device identification

Trade name: WorkPark WP 1 Work shelf
UDI-DI code: 04260101482006
Basic UDI-DI: B-04260101482006
Reference / catalog number: 1621510
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Device for use in occupational therapy and work simulation training. It enables structured exercises for assessing activity and functional capabilities. Evaluation and interpretation are performed by qualified professionals and are not part of the device.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - 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

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