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Silcatrise Gel

EUDAMED

Class I (EU MDR)

Ref Silcatrise Gel 10g

by M-Technologies

Identity

Trade Name
Silcatrise Gel EUDAMED
Device Name
Silcatrise Gel 10g EUDAMED
Model / Reference
Silcatrise Gel 10g EUDAMED

Identifiers

Primary DI / UDI-DI
03760347221632 EUDAMED
Basic UDI-DI
B-03760347221632 EUDAMED
EMDN Code
M04040701 SILICONE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Silcatrise Gel by M-Technologies — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
M-Technologies
EUDAMED SRN
FR-MF-000016995

Sources (1)

  • EUDAMED 29efdfd7-8f8b-4679-9a80-c1c465726319 61 fields · synced Jul 20, 2026