Rhinomer
by Laboratoire de la Mer 2 variants
Ref OH1301020, OH1255020Model LABMER-002/D-01, LABMER-004/C-01
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/MDR | NumberB-03564300032897 | Date3 Apr 2024 | StatusActive |
| European Union | CE/MDD | NumberB-03564300032897 | Date3 Apr 2024 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Device Name
- RHINOMER DE PLUS 22gr/l 20mlSeawater-based osmotic nasal decongestant with aroma in metered pump (PRD0915)
- Model / Reference
- LABMER-002/D-01, OH1301020, LABMER-004/C-01, OH1255020
- Primary DI / UDI-DI
- 03564300032897, 08470001621917
- Basic UDI-DI
- B-03564300032897, 356430LABMER-004/C-HC
- EMDN Code
- Q030103, Q030199
- Device Class
- Class IClass IIa
- EU market of registration
- GermanySpain
Manufacturer details
- EUDAMED SRN
- FR-MF-000009050
Other devices from Laboratoire de la Mer
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No