Aurora Boreale
by Aqua Medi̇kal Tibbi̇ Araç Ve Gereç İnş. San. Diş Ti̇c. Ltd. Şti̇. 2 variants
Ref LUB-50
Active
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 | NumberB-08684936800556 08684936800556 | Date30 Jun 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- Withdrawn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 Active
Specification
- Device Name
- Aurora Boreale Lubricant Gel 50 ml
- Model / Reference
- LUB-50
- Primary DI / UDI-DI
- 08684936800556
- Basic UDI-DI
- B-08684936800556
- EMDN Code
- V0399 Measurement devices - other
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000023642
Other devices from Aqua Medi̇kal Tibbi̇ Araç Ve Gereç İnş. San. Diş Ti̇c. Ltd. Şti̇.
See all devices from Aqua Medi̇kal Tibbi̇ Araç Ve Gereç İnş. San. Diş Ti̇c. Ltd. Şti̇. →
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No