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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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TUR Inserts — 5 UDI-DI variants, MDR (Eurotape B.V.)

MD Atlas
Eurotape B.V.

Data from EUDAMED, last updated May 30, 2026

TUR Inserts

871992590100TEX

5 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: Eurotape B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871992590100TEX
Device name: TUR Inserts
Device model: TUR Inserts
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Eurotape B.V.
SRN: NL-MF-000001956
Country: Netherlands
Email: info@eurotape.com
Phone: +31356091020

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FS21N7585GKD4VKDK60DXKA7

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

Med/TUR E05 LF08719925900518
Med/TUR E10 LF08719925900525
Med/TUR03 E10 LF08719925900556
Med/TUR175 E10 LF08719925900563
Med/TUR175 E18 LF08719925900570