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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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Relegs Electrode patches — 1 UDI-DI variant, MDR (RELEGS BV)

MD Atlas
RELEGS BV

Data from EUDAMED, last updated May 30, 2026

Relegs Electrode patches

87193275088RP-001AMN

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: RELEGS BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87193275088RP-001AMN
Device name: Relegs Electrode patches
Device model: 1140
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: RELEGS BV
SRN: NL-MF-000005880
Country: Netherlands
Email: support@relegs.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GCC0SDCWKJX57CAAZWZWX5PC

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

114008719327508800