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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

Eurogel plus 10g — Class I MDD by M-Technologies

MD Atlas
M-Technologies

EUDAMED last updated this device on Jul 8, 2025

Eurogel plus 10g

B-03760347221571

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: M-Technologies
UDI-DI code: 03760347221571
Reference / catalog number: Eurogel plus 10g

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Manufacturer information

Organization name: M-Technologies
SRN: FR-MF-000016995
Manufacturer status: Active

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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.

Critical warnings

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

CW262
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Hungary		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760347221571
Basic UDI-DI: B-03760347221571
Reference / catalog number: Eurogel plus 10g
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Silicone gel for scar treatment
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10 MU24

EMDN nomenclature code(s)

M04040701SILICONE DRESSINGS, NON-COMBINED

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