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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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Neuromuscular electrical stimulator… — 2 UDI-DI variants, MDR

MD Atlas
Verity Medical Ltd.

Data from EUDAMED, last updated May 24, 2026

Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered

506007397ETS2004C

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: Verity Medical Ltd.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 506007397ETS2004C
Device name: Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: Verity Medical Ltd.
SRN: IE-MF-000007426
Country: Ireland
Email: sales@veritymedical.com
Phone: +353(0)539132433

Variants by status

UDI-DI variants

2 UDI-DI variants

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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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