Portable Mesh Nebulizer
by Feellife Health Inc. 40 variants
Ref Air Mask
Active
CE MDR CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | Number69343253R06010120A7Y 06934325303567 | Date22 Apr 2026 | StatusActive |
| European Union | CE/MDR | Number69343253R06010120A7Y 06934325303567 | Date22 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Trade Name
- feellife
- Device Name
- Portable Mesh Nebulizer
- Model / Reference
- Air Mask
- Primary DI / UDI-DI
- 06934325303567
- Basic UDI-DI
- 69343253R06010120A7Y, B-06934325303567
- Direct Marketing DI
- 06934325303567
- EMDN Code
- R060101 Cold nebulisation systems
- Device Class
- Class IIa
- EU market of registration
- AustriaItaly
Manufacturer details
- EUDAMED SRN
- CN-MF-000000782
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Feellife Health Inc.
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Measuring Function: No
- Incorporates Medicinal Product: No