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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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Bathtub seat SWIVEL standard seat — 1 UDI-DI variant, MDR

MD Atlas
Nordic activity AB

Data from EUDAMED, last updated May 30, 2026

Bathtub seat SWIVEL standard seat

73500849733673F

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: Nordic activity AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73500849733673F
Device name: Bathtub seat SWIVEL standard seat
Device model: 1-1136
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Nordic activity AB
SRN: SE-MF-000002371
Country: Sweden
Email: nordic@nordicactivity.se
Phone: +46 42-147860

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01GW4819BKP5G2PTZYDJX3HTXP

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

GB-2023-0107350084973367