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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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Tellus i6 — 6 UDI-DI variants, MDR (Jabbla)

MD Atlas
Jabbla

Data from EUDAMED, last updated May 23, 2026

Tellus i6

5430000266SGDVP

6 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: Jabbla

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430000266SGDVP
Device name: Tellus i6
Device model: Tellus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Jabbla
SRN: BE-MF-000049893
Country: Belgium
Email: bart.noe@jabbla.com
Phone: +3293315858

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRXEJYT0JE03260BQ1BZCBTV

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

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HeyPad54300002668026
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Tellus i654300002668712
Vibe 1054300002668644
Vibe 12+54300002668330