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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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ReLink Drain — 1 UDI-DI variant, MDR (Interlinked AB)

MD Atlas
Interlinked AB

Data from EUDAMED, last updated May 31, 2026

ReLink Drain

735012805ReLinkDrainDS

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: Interlinked AB

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 735012805ReLinkDrainDS
Device name: ReLink Drain
Device model: ReLink Drain 1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Interlinked AB
SRN: SE-MF-000040455
Country: Sweden
Email: info@interlinked.care
Phone: + 46 70 342 48 20

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRBJWFEGA8FBDQXVVTEB2TYF

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

ReLink Drain 107350128050191