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Again Pro Plus

EUDAMED

Class IIb (EU MDR)

Ref M126S1

by Deka M.e.l.a. Srl

Identity

Trade Name
AGAIN PRO PLUS EUDAMED
Device Name
AGAIN EUDAMED
Model / Reference
M126S1 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108512372 EUDAMED
Basic UDI-DI
B-08034108512372 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

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

Again Pro Plus by Deka M.e.l.a. Srl — Class IIb — 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
Deka M.e.l.a. Srl
EUDAMED SRN
IT-MF-000007389

Sources (1)

  • EUDAMED e195f4fc-3ab4-4806-88ea-fc626693f675 61 fields · synced Jun 19, 2026