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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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ITS Terra 100 — 9 UDI-DI variants, MDR (Starmed)

MD Atlas
Starmed

Data from EUDAMED, last updated May 23, 2026

ITS Terra 100

426051502ITSDG

9 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: Starmed

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426051502ITSDG
Device name: ITS Terra 100
Device model: ITS Terra 100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: Starmed
SRN: DE-MF-000026331
Country: Germany
Email: info@starmed.eu
Phone: +49 (0) 7532 445990 0

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01H003AJK6XDHQFN8W9P5FSMQ9

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

ITS Terra 10004260515020030
ITS Terra 10004260515020092
ITS Terra 10004260515020047
02-010-000904260515020061
ITS Terra 10004260515020023
ITS Terra 10004260515020085
02-010-001404260515020016
ITS Terra 10004260515020054
ITS Terra 10004260515020078