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Excilite μ

EUDAMED

Class IIb (EU MDR)

Ref M083A2

by Deka M.e.l.a. Srl

Identity

Trade Name
Excilite μ EUDAMED
Device Name
Excilite μ EUDAMED
Model / Reference
M083A2 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108510378 EUDAMED
Basic UDI-DI
B-08034108510378 EUDAMED
803410851M083XXRV EUDAMED
EMDN Code
Z12040202 PHOTOTHERAPY EQUIPMENT 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

Category: Red-light phototherapy unit, professional

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

Similar devices

Also classified as Red-light phototherapy unit, professional.

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 f8d8148f-68dc-417f-aaae-98e93401f52a 61 fields · synced Jul 22, 2026
  • EUDAMED 4c72c761-8dbd-46e4-a894-db77670fc44b 61 fields · synced May 18, 2026