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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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esense Line — 8 UDI-DI variants, MDR (Indes Healthcare BV)

MD Atlas
Indes Healthcare BV

Data from EUDAMED, last updated May 30, 2026

esense Line

87202994521LINE3X

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: Indes Healthcare BV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 87202994521LINE3X
Device name: esense Line
Device model: esense Line
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: Indes Healthcare BV
SRN: NL-MF-000000051
Country: Netherlands
Email: info@indes.eu
Phone: 0031-53-4803920

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01G5GR8N02MQ85RX32JSW5AXJ2

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

esense Line08720299452107
esense Line+08720299452114
esense Line20008720299452121
esense Line23008720299452138
SlingCare Straight08720299452145
SlingCare Straight Max08720299452183
SlingCare Straight Up08720299452152
SlingCare Straight Up 20008720299452190