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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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TWIST — 10 UDI-DI variants, MDR (KLAXON MOBILITY GmbH)

MD Atlas
KLAXON MOBILITY GmbH

Data from EUDAMED, last updated May 23, 2026

TWIST

918000246TWIST2022HF

10 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: KLAXON MOBILITY GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 918000246TWIST2022HF
Device name: TWIST
Device model: TWIST
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: KLAXON MOBILITY GmbH
SRN: AT-MF-000004590
Country: Austria
Email: info.klaxon@etac.com
Phone: +436644681294

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K60RKC6D2Y9YNYYQ0V3BXVP3

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

TWIST09180002464084
TWIST09180002464107
TWIST09180002464091
TWIST09180002464060
TWIST09180002464053
TWIST09180002463773
TWIST09180002463797
TWIST09180002463780
TWIST09180002463766
TWIST09180002464077