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Sutricon

EUDAMED

Class I (EU MDR)

Ref Sutricon 3*10Ref Sutricon 5*30

by M-Technologies

Identity

Trade Name
Sutricon EUDAMED
Device Name
Sutricon 3*10 EUDAMED
Sutricon 5*30 EUDAMED
Model / Reference
Sutricon 3*10 EUDAMED
Sutricon 5*30 EUDAMED

Identifiers

Primary DI / UDI-DI
03760347221755 EUDAMED
03760347221762 EUDAMED
Basic UDI-DI
B-03760347221755 EUDAMED
B-03760347221762 EUDAMED
EMDN Code
M04040701 SILICONE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Sutricon 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 (2)

  • EUDAMED 2af91655-e175-40bc-9ce3-5ab120dce3f9 61 fields · synced Jul 16, 2026
  • EUDAMED be8cdb27-7e7c-4738-92c8-70eb5e3e18a6 61 fields · synced May 18, 2026