← Back to catalogue

Red Touch Pro

EUDAMED

Class IIb (EU MDR)

Ref M121G1

by Deka M.e.l.a. Srl

Identity

Trade Name
RED TOUCH PRO EUDAMED
Device Name
RED TOUCH EUDAMED
Model / Reference
M121G1 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108512198 EUDAMED
Basic UDI-DI
B-08034108512198 EUDAMED
EMDN Code
Z12011016 DIODE 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

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

Red Touch Pro 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED c9aea6ed-aaff-4550-beaa-5833129197e1 61 fields · synced Aug 3, 2026