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LazuLymph

EUDAMED

Class IIa (EU MDR)

Ref MBPA2502

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

Identity

Trade Name
LazuLymph EUDAMED
Device Name
LazuLymph EUDAMED
Model / Reference
MBPA2502 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742102810 EUDAMED
08052742103893 EUDAMED
Basic UDI-DI
805274210LazuLy22 EUDAMED
Unit of Use DI
18052742102817 EUDAMED
18052742103890 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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 (2)

  • EUDAMED 8033c52a-932c-4112-9a4d-067056eb2831 61 fields · synced Oct 6, 2026
  • EUDAMED bc077fc3-de64-4d4e-9e54-c4b2e5a52793 61 fields · synced May 19, 2026