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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

TR Comfortline Bath, with… — Class I MDR by TR Equipment AB

MD Atlas
TR Equipment AB

EUDAMED last updated this device on May 27, 2026

TR Comfortline Bath, with Rohrunterbrecher, 50 mm drainage

7350016060206C

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TR Equipment AB
UDI-DI code: 07350016061674
Reference / catalog number: 05194006

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View device family (Basic UDI)

Manufacturer information

Organization name: TR Equipment AB
SRN: SE-MF-000027486
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Lithuania; available across 2 countries total.

Country	On market since	Until
LithuaniaPrimary placement	Jan 1, 2011	Still on market
Sweden	Jan 1, 2011	Still on market

Device identification

Trade name: TR Comfortline Bath, with Rohrunterbrecher, 50 mm drainage
UDI-DI code: 07350016061674
Basic UDI-DI: 7350016060206C
Reference / catalog number: 05194006
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: https://www.trequipment.com/product/bathtub-tr-comfortline/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350016061674

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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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.