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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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actiTENS / VitaliTENS — 7 UDI-DI variants, MDR (SUBLIMED)

MD Atlas
SUBLIMED

Data from EUDAMED, last updated May 19, 2026

actiTENS / VitaliTENS

3770018808SBMTENSAPPNU

7 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: SUBLIMED

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770018808SBMTENSAPPNU
Device name: actiTENS / VitaliTENS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: SUBLIMED
SRN: FR-MF-000007546
Country: France
Email: PRRC-Sublimed@subli-med.com
Phone: +33476371758

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H3M5F9J88QXN93XW9CP9VV22

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

actiTENS Android appB786SBM2AA1000
actiTENS iOS appB786SBM2AA2000
SBM7AA10003770018808260
Application mobile VitaliTENS pour AndroidB786EXP2AA1000
Application mobile VitaliTENS pour iOSB786EXP2AA2000
VitaliTENS03770018808055
870442703770018808291