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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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Organization name
UDI-DI code
Reference / catalog number

Brassard VitaliTENS Taille XL — Class I MDR by SUBLIMED

MD Atlas
SUBLIMED

EUDAMED last updated this device on Sep 3, 2025

Brassard VitaliTENS Taille XL

3770018808ATVitaliTENS1PK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SUBLIMED
UDI-DI code: 03770018808017
Reference / catalog number: 8703699

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Manufacturer information

Organization name: SUBLIMED
SRN: FR-MF-000007546
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Aug 29, 2022	Still on market

Device identification

Trade name: Brassard VitaliTENS Taille XL
UDI-DI code: 03770018808017
Basic UDI-DI: 3770018808ATVitaliTENS1PK
Reference / catalog number: 8703699
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Le GIE VitaliTENS peut être maintenu sur le corps du patient grâce à un accessoire textile. Les brassards sont destinés à être placés sur n'importe quelle partie du corps mais pas sur une peau blessée ou irritée. Le but des accessoires textiles est de maintenir le GIE VitaliTENS à proximité de la partie du corps que le patient souhaite stimuler.
Additional information URL: https://subli-med.com/wp-content/uploads/2017/11/Xp/Notice.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120601ELECTROTHERAPY EQUIPMENT (INCLUDED TENS)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.