← Back to catalogue
Allux Dual
EUDAMEDClass IIb (EU MDR)
Ref AMI-CL-0611Model ALLUX DUAL
by Ami Inc.
Identity
- Trade Name
- ALLUX DUAL EUDAMED
- Device Name
- Alexandrite & Long Pulsed Nd:YAG Laser EUDAMED
- Model / Reference
- ALLUX DUAL EUDAMEDAMI-CL-0611 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08800042100032 EUDAMED
- Basic UDI-DI
- B-08800042100032 EUDAMED
- EMDN Code
- Z12011012 DYE/ALEXANDRITE SURGICAL LASER EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Lithuania EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
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
Allux Dual by Ami Inc. — Class IIb — 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-08800042100032 | Class IIb | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ami Inc.
- EUDAMED SRN
- KR-MF-000017522
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED 298964ae-a850-4d4f-b32d-8e56ac1606e0 61 fields · synced Sep 17, 2026