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Solis 130fa

EUDAMED

Class I (EU MDR)

Ref SOLIS 160FA

by FAE Famed Łódź S.A.

Identity

Trade Name
SOLIS 130FA EUDAMED
Device Name
SOLIS 130 Lampa operacyjna EUDAMED
Model / Reference
SOLIS 160FA EUDAMED

Identifiers

Primary DI / UDI-DI
05904708713444 EUDAMED
Basic UDI-DI
5904708713SOLIS130A8 EUDAMED
Direct Marketing DI
05904708713444 EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Solis 130fa by FAE Famed Łódź S.A. — Class I — 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

EUDAMED SRN
PL-MF-000018775

Sources (1)

  • EUDAMED 6842002e-fb12-420c-bac9-923b6e730506 61 fields · synced Jun 18, 2026