Identity
- Trade Name
- Huf Puf Kit EUDAMED
- Device Name
- Huf Puf Kit (spacer + mask) EUDAMED
- Model / Reference
- Not Applicable for Huf Puf Kit EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-8901117HPK0123KYQM EUDAMED
- Basic UDI-DI
- B-8901117HPK0123KYQM EUDAMED
- EMDN Code
- R03010399 AEROSOL THERAPY SYSTEMS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Huf Puf Kit by Cipla Limited — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-8901117HPK0123KYQM | Class I | No Longer Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cipla Limited
- EUDAMED SRN
- IN-MF-000038939
- Authorised Representative
- Cipla Europe NV BE-AR-000038918
Sources (1)
- EUDAMED 63170335-84d0-4c1a-abef-8b05b60000d2 61 fields · synced Jul 9, 2026