Identity
- Trade Name
- FLORE Lidocaine EUDAMED
- Device Name
- Cross-linked Hyaluronate Acid Dermal Filler with Lidocaine EUDAMED
- Model / Reference
- CL-Strong EUDAMEDLL2St EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809369092983 EUDAMED
- Basic UDI-DI
- B-08809369092983 EUDAMED
- EMDN Code
- P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
FLORE Lidocaine by BNC KOREA, Inc. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809369092983 | Class III | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BNC KOREA, Inc.
- EUDAMED SRN
- KR-MF-000008321
- Authorised Representative
- JaviTech e.K. DE-AR-000005875
Sources (1)
- EUDAMED f2dcf63f-e7f9-4409-b226-40ae1e441283 61 fields · synced Jun 18, 2026