← Back to catalogue

Fluosoft Lm

EUDAMED

Class IIa (EU MDR)

Ref FSLM-CL

by Fluoptics Sas

Identity

Trade Name
FLUOSOFT LM EUDAMED
Device Name
FLUOSOFT LX/LM EUDAMED
Model / Reference
FSLM-CL EUDAMED

Identifiers

Primary DI / UDI-DI
+B475FSLM-CL0 EUDAMED
Basic UDI-DI
++B475FSAG EUDAMED
EMDN Code
Z119082 VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
France 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

Fluosoft Lm by Fluoptics Sas — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

Manufacturer
Fluoptics Sas
EUDAMED SRN
FR-MF-000000403

Sources (1)

  • EUDAMED b939ae34-206f-4717-be67-0699f332e356 61 fields · synced Jul 9, 2026