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LASEmaR 1000

EUDAMED

Class IIb (EU MDR)

Ref LASEmaR 1000Model LASEmaR

by Eufoton Srl

Identity

Trade Name
LASEmaR 1000 EUDAMED
Device Name
LASEmaR EUDAMED
Model / Reference
LASEmaR EUDAMED
LASEmaR 1000 EUDAMED

Identifiers

Primary DI / UDI-DI
08054188640543 EUDAMED
Basic UDI-DI
805418864LASEMAR4GMB EUDAMED
Direct Marketing DI
08054188640543 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

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

LASEmaR 1000 by Eufoton 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
Eufoton Srl
EUDAMED SRN
IT-MF-000009227

Sources (1)

  • EUDAMED c169a7fb-d6e3-4496-8f84-dd291a6cd918 61 fields · synced May 23, 2026