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HiScan DOT/RF

EUDAMED

Class IIb (EU MDR)

Ref F26901

by Deka M.e.l.a. Srl

Identity

Trade Name
HiScan DOT/RF EUDAMED
Device Name
Scanning units for CO2 lasers EUDAMED
Model / Reference
F26901 EUDAMED

Identifiers

Primary DI / UDI-DI
08034108511313 EUDAMED
Basic UDI-DI
803410851F49801KD EUDAMED
EMDN Code
Z12011099 LASER SURGERY INSTRUMENTS - OTHER 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

HiScan DOT/RF by Deka M.e.l.a. Srl — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED a98a6aa7-1c06-4a78-a6fd-95ea6c21c6c7 61 fields · synced Jun 18, 2026