Soro Fisiológico Dimor 500 mL
by Alliande - Expert Manufacturer, Lda
Ref P2100006
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Overview
The Soro Fisiológico Dimor 500 mL medical device is a Class I device, designed for the treatment of respiratory conditions. It uses Alliande - Expert Manufacturer, Lda as its manufacturer and has undergone comprehensive testing to ensure its safety and efficacy.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5600221488P02Y24K8 05600221488028 | Date25 Jun 2024 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- P2100006
- Primary DI / UDI-DI
- 05600221488028
- Basic UDI-DI
- 5600221488P02Y24K8
- EMDN Code
- Q030103 Nasal irrigation solutions
- Device Class
- Class I
- EU market of registration
- Portugal
Manufacturer details
- EUDAMED SRN
- PT-MF-000029328
Other devices from Alliande - Expert Manufacturer, Lda
Properties
Other properties (13)
- 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
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No