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Leepak
EUDAMEDClass IIa (EU MDR)
Ref 64Model Sodium Chloride Inhalation Solution 0.9% w/v 2.5 ML
Identity
- Trade Name
- LEEPAK EUDAMED
- Device Name
- Sodium Chloride Inhalation Solution 0.9% w/v EUDAMED
- Model / Reference
- Sodium Chloride Inhalation Solution 0.9% w/v 2.5 ML EUDAMED64 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G4996414 EUDAMED
- Basic UDI-DI
- B-G4996414 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-G4996414 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Legency Remedies Pvt. Ltd.
- EUDAMED SRN
- IN-MF-000010030
- Authorised Representative
- Europecert UG (haftungsbeschränkt) DE-AR-000004974
Sources (1)
- EUDAMED a0c1469f-8628-4201-b4db-e4c0556baf47 61 fields · synced Jun 18, 2026