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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

915109 — Class I MDR by ADHEX TECHNOLOGIES SAS

MD Atlas
ADHEX TECHNOLOGIES SAS

EUDAMED last updated this device on Jan 20, 2026

915109

376033917TIPSTOPEUROPELB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ADHEX TECHNOLOGIES SAS
UDI-DI code: 03760339171228
Reference / catalog number: 915109

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Manufacturer information

Organization name: ADHEX TECHNOLOGIES SAS
SRN: FR-MF-000009493
Manufacturer status: Active

Critical warnings

6 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW999
Contre indiqué chez les patients allergiques à l'aginate. N'est pas destiné à être utilisé sur des brulures du 3eme degré ou sur des plaies profondes. N'est pas destiné à être utilisé de façon prolongé ou permanente. N'a pas été conçu pour être utilisé en tant que peau artificielle ou synthétique. N'est pas destiné au traitement des ulcères de stase vasculaire. Contre-indiqué pour la population pédiatrique.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Oct 29, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760339171228
Basic UDI-DI: 376033917TIPSTOPEUROPELB
Reference / catalog number: 915109
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: 200
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030404DIALYSIS FISTULA, BANDAGES

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

Related devices

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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.