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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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Bidet — 1 UDI-DI variant, MDR (RowLAM Sp. z o.o.)

MD Atlas
RowLAM Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

Bidet

5905279578BIDETMEDBH

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: RowLAM Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5905279578BIDETMEDBH
Device name: Bidet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: RowLAM Sp. z o.o.
SRN: PL-MF-000025857
Country: Poland
Email: rowlam@rowlam.com.pl
Phone: +48 62 764 55 08

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JJKA7HVCVND7ZCSS7TPBFKBV

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

BN05905279578227