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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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ReShell — 8 UDI-DI variants, MDR (LC Seating LTD)

MD Atlas
LC Seating LTD

Data from EUDAMED, last updated May 24, 2026

ReShell

539154948RSFAMN2

8 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: LC Seating LTD

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 539154948RSFAMN2
Device name: ReShell
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: LC Seating LTD
SRN: IE-MF-000048326
Country: Ireland
Email: info@lcs.ltd
Phone: +353719163905

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KRGYQYH2G7PM2JT83X0RC48P

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

Reshell05391549480015
ReShell05391549480084
ReShell05391549480077
ReShell05391549480060
ReShell05391549480046
ReShell05391549480053
ReShell05391549480022
ReShell05391549480039