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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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DekoRen+ Tørr — 2 UDI-DI variants, MDR (Lilleborg AS)

MD Atlas
Lilleborg AS

Data from EUDAMED, last updated May 30, 2026

DekoRen+ Tørr

704611DEKORENTORRH6

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: Lilleborg AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 704611DEKORENTORRH6
Device name: DekoRen+ Tørr
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: Lilleborg AS
SRN: NO-MF-000012956
Country: Norway
Email: kundeservice.lilleborg@solenis.com
Phone: +4781536000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FZFQP78BRCYX1BPS5EMHMQXY

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

373707046110217580
383207046110220528