← Back to catalogue

Leeneb

EUDAMED

Class IIa (EU MDR)

Ref 142

by Legency Remedies Pvt. Ltd.

Identity

Trade Name
LEENEB EUDAMED
Device Name
Sodium Chloride Inhalation Solution 0.9% w/v 20ml EUDAMED
Model / Reference
142 EUDAMED

Identifiers

Primary DI / UDI-DI
D-142salinesolutionTY EUDAMED
Basic UDI-DI
B-142salinesolutionTY 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

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

Manufacturer

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

Sources (1)

  • EUDAMED 0e5ed1a0-782c-4d30-9242-cd26d113ac0e 61 fields · synced Jul 13, 2026