Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Activ'M Gel 10g — Class IIa MDR by M-Technologies

MD Atlas
M-Technologies

EUDAMED last updated this device on Jul 15, 2025

Activ'M Gel 10g

376034722GEL10012G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M-Technologies
UDI-DI code: 03760347221212
Reference / catalog number: Activ'M Gel 10g

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

Activ'M Gel 10gB-03760347221212On the market Activ'M Gel 20gB-03760347221540On the market Activ'M Gel 15gB-03760347221168On the market Activ'M Gel 3in1 10gB-03760347221656On the market Activ'M Gel SPF 10g376034722GELSPF2001Q8On the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW262
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
Belgium		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760347221212
Basic UDI-DI: 376034722GEL10012G
Reference / catalog number: Activ'M Gel 10g
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 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

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.