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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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Inserts — 36 UDI-DI variants, MDR (Eurotape B.V.)

MD Atlas
Eurotape B.V.

Data from EUDAMED, last updated May 30, 2026

Inserts

871992590100IE9

36 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: 871992590100IE9
Device name: Inserts
Device model: 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

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FS21N2A1E1Q35HY3FF42SW8T

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

SteriStretch® 30-3008719925905124
SteriStretch® 30-3508719925905148
SteriStretch® 30-4208719925905162
SteriStretch® 30-6508719925905186
SteriStretch® 35-3008719925905209
SteriStretch® 35-4208719925905230
SteriStretch® 35-6508719925905261
SteriStretch® 35-8008719925905285
SteriStretch® 3940-14008719925905308
SteriStretch® 4060-1508719925905339
SteriStretch® 4060-1908719925905377

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