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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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Torso Applicator — 2 UDI-DI variants, MDR (Novocure GmbH)

MD Atlas
Novocure GmbH

Data from EUDAMED, last updated May 23, 2026

Torso Applicator

0729010798ACM3H

2 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: Novocure GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0729010798ACM3H
Device name: Torso Applicator
Device model: ACM00010
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: Novocure GmbH
SRN: CH-MF-000029002
Country: Switzerland
Email: info@novocure.com

Authorised representative

Name: MDSS GmbH
SRN: DE-AR-000005430
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J30GECQZCD3TJF4C8H29SAQ9

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

Torso Applicator07290107986892
Torso Applicator07290107986908