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LazuLymph

EUDAMED

Class IIa (EU MDR)

Ref MBPS2502

by S.A.L.F. S.p.A. Laboratorio Farmacologico

Identity

Trade Name
LazuLymph EUDAMED
Device Name
LazuLymph EUDAMED
Model / Reference
MBPS2502 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742104135 EUDAMED
Basic UDI-DI
805274210LazuLy22 EUDAMED
Unit of Use DI
18052742104132 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Hungary EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Device sterilization/disinfection container, reusable

LazuLymph by S.A.L.F. S.p.A. Laboratorio Farmacologico — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000010720

Sources (1)

  • EUDAMED 3559fa10-8461-4602-aa16-2dd427cae0c5 61 fields · synced Jun 19, 2026