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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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AXION TENS Devices — 2 UDI-DI variants, MDR (axion GmbH)

MD Atlas
axion GmbH

Data from EUDAMED, last updated May 23, 2026

AXION TENS Devices

426028018TENS9B

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: axion GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426028018TENS9B
Device name: AXION TENS Devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: axion GmbH
SRN: DE-MF-000006487
Country: Germany
Email: service@axion-net.de
Phone: +4971523539110

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNA613JW9GN2GPY3Q0F3HQR

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

102304260280181318
101404260280180724