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Smartxide2 Trio C60h

EUDAMED

Class IIb (EU MDR)

Ref M103AJ1

by Deka M.e.l.a. Srl

Identity

Trade Name
SMARTXIDE2 TRIO C60H EUDAMED
Device Name
SMARTXIDE2 TRIO C60H EUDAMED
Smartxide2 family EUDAMED
Model / Reference
M103AJ1 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108510903 EUDAMED
Basic UDI-DI
B-08034108510903 EUDAMED
803410851M103XXQG EUDAMED
EMDN Code
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 Trio C60h 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 51ed2dc7-c298-40cd-add3-2a7433fcbd6d 61 fields · synced Jul 17, 2026
  • EUDAMED aa85c1d7-fe9f-4873-b71c-5f83ec4f1b21 61 fields · synced May 19, 2026