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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

BACKREST FOR BATHTUB SEAT KING — Class I MDR

MD Atlas
LM Global Design Limited

EUDAMED last updated this device on Mar 19, 2025

BACKREST FOR BATHTUB SEAT KING

539154872LMBSJC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LM Global Design Limited
UDI-DI code: 05391548723816
Reference / catalog number: KING-BR-KN

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Manufacturer information

Organization name: LM Global Design Limited
SRN: IE-MF-000046744
Manufacturer status: Active

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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.

Critical warnings

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

CW010
Safety and Warning Indications

Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: BACKREST FOR BATHTUB SEAT KING
UDI-DI code: 05391548723816
Basic UDI-DI: 539154872LMBSJC
Reference / catalog number: KING-BR-KN
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: This product is an accessory for the KING Bathtub Seats family
Additional information URL: https://kingbathrooms.com/products/backrest-for-bathtub-seat/?portfolioCats=50%2C49
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y093399WASHING, BATHING AND SHOWERING DEVICES - 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
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Software identification