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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

Saljol Duschhocker DH51 Diamond… — Class I MDR by Saljol GmbH

MD Atlas
Saljol GmbH

EUDAMED last updated this device on Jul 21, 2023

Saljol Duschhocker DH51 Diamond Silver

4058789SaljolHocker6W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Saljol GmbH
UDI-DI code: 04058789014370
Reference / catalog number: Saljol Duschhocker DH51 Diamond Silver

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Manufacturer information

Organization name: Saljol GmbH
SRN: DE-MF-000015913
Manufacturer status: Active

Critical warnings

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

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: 04058789014370
Basic UDI-DI: 4058789SaljolHocker6W
Reference / catalog number: Saljol Duschhocker DH51 Diamond Silver
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: The shower stool from Saljol was developed for home and stationary areas, mainly for use in shower/washing rooms. For people with limited mobility it serves as a shower aid with four wheels for independent showering/washing and sitting.
Additional information URL: https://www.saljol.de/de/saljol-duschhocker/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y093303FIXED AND ROTARY CHAIRS FOR BATH AND SHOWER

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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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.