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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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Klara RIK-sits för kateterisering — 2 UDI-DI variants, MDR

MD Atlas
Svan Care AB

Data from EUDAMED, last updated May 31, 2026

Klara RIK-sits för kateterisering

7350011590567C

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Svan Care AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 7350011590567C
Device name: —
Device model: Klara RIK-sits för kateterisering
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Svan Care AB
SRN: SE-MF-000049398
Country: Sweden
Email: info@svancare.se
Phone: +46 240 10102

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS62ZY5QXGP1Y7DGACE1BDNK

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

1017273500115905277
1017173500115905673