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Smartxide2 C80

EUDAMED

Class IIb (EU MDR)

Ref M103E1

by Deka M.e.l.a. Srl

Identity

Trade Name
Smartxide2 C80 EUDAMED
Device Name
Smartxide2 C80 EUDAMED
Smartxide2 family EUDAMED
Model / Reference
M103E1 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108510453 EUDAMED
Basic UDI-DI
B-08034108510453 EUDAMED
803410851M103XXQG EUDAMED
EMDN Code
Z12011005 CARBON DIOXIDE SURGICAL LASER EUDAMED
Z12011019 MULTI–PLATFORM 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

Smartxide2 C80 by Deka M.e.l.a. Srl — Class IIb — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 3f77b94f-901e-46c7-b77e-1c3fd6a454d1 61 fields · synced Jul 16, 2026
  • EUDAMED 1dd1f52c-d177-483a-aa29-d98109b39d90 61 fields · synced May 19, 2026