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Nanosoft

EUDAMED

Class IIa (EU MDR)

Ref AS4053Model Micronjet600

by NanoPass Technologies Ltd.

Identity

Trade Name
Nanosoft EUDAMED
Device Name
Micronjet EUDAMED
Model / Reference
Micronjet600 EUDAMED
AS4053 EUDAMED

Identifiers

Primary DI / UDI-DI
17290015928233 EUDAMED
Basic UDI-DI
729001592803C3 EUDAMED
EMDN Code
A01010199 HYPODERMIC NEEDLES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Nanosoft by Nanopass Technologies Ltd. — Class IIa — 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
IL-MF-000023415
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED f1f9a692-2912-4e73-b14c-f565ea420de0 61 fields · synced Jul 10, 2026