← Back to catalogue

Leepak

EUDAMED

Class IIa (EU MDR)

Ref 135

by Legency Remedies Pvt. Ltd.

Identity

Trade Name
LEEPAK EUDAMED
Device Name
Sodium Chloride Inhalation Solution 0.9% w/v 5ml EUDAMED
Model / Reference
135 EUDAMED

Identifiers

Primary DI / UDI-DI
D-salinesolution135J9 EUDAMED
Basic UDI-DI
B-salinesolution135J9 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

Leepak 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 f3bbb2d4-669a-48ad-b94a-4fb64eff94ec 61 fields · synced Jun 19, 2026