Idroflog
by Alfa Intes Industria Terapeutica Splendore S.r.l. 16 variants
Ref 5010151
Active
CE MDR
Valid until
13 Jun 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number805848137IDROFLOGMDKU 08058481370695 | Date8 Jul 2026 | StatusActive |
Certificates
- CSQ0023240326 Active
Quality management system EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 3 Jul 2026
- Expires
- 13 Jun 2029
- Reason
- Add device or group
- CVD0029240126 Active
Technical documentation EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 3 Jul 2026
- Expires
- 13 Jun 2029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- 5010151
- Primary DI / UDI-DI
- 08058481370695
- Basic UDI-DI
- 805848137IDROFLOGMDKU
- EMDN Code
- Q02030206 Eye lubricant solutions
- Device Class
- Class III
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- IT-MF-000025980
Other devices from Alfa Intes Industria Terapeutica Splendore S.r.l.
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Properties
Other properties (11)
- 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