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Smartxide

EUDAMED

Class IIb (EU MDR)

Ref M079C1

by Deka M.e.l.a. Srl

Identity

Trade Name
SMARTXIDE EUDAMED
Device Name
SMARTXIDE family EUDAMED
SMARTXIDE EUDAMED
Model / Reference
M079C1 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108510491 EUDAMED
Basic UDI-DI
803410851M079XXSL EUDAMED
B-08034108510491 EUDAMED
EMDN Code
Z12011005 CARBON DIOXIDE SURGICAL LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Smartxide by Deka M.e.l.a. Srl — Class IIb — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Deka M.e.l.a. Srl
EUDAMED SRN
IT-MF-000007389

Sources (2)

  • EUDAMED 8bfaacee-fab8-4339-aad4-5157ab961d48 61 fields · synced Jul 14, 2026
  • EUDAMED 489399b2-d06e-481f-b260-02e5d300077c 61 fields · synced May 19, 2026