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Leeneb

EUDAMED

Class IIa (EU MDR)

Ref 42

by Legency Remedies Pvt. Ltd.

Identity

Trade Name
LEENEB EUDAMED
Device Name
Sodium Chloride Inhalation Solution 0.9% w/v 2ml EUDAMED
Model / Reference
42 EUDAMED

Identifiers

Primary DI / UDI-DI
D-42salinesolution26 EUDAMED
Basic UDI-DI
B-42salinesolution26 EUDAMED
EMDN Code
R060203 INHALATION THERAPY HUMIDIFICATION LIQUIDS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Leeneb by Legency Remedies Pvt. Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000010030
Authorised Representative
Europecert UG (haftungsbeschränkt) DE-AR-000004974

Sources (1)

  • EUDAMED 9483af8a-f125-47dd-bbce-04cefd35c452 61 fields · synced Jun 19, 2026