Identity
- Trade Name
- AD PLUS EUDAMED
- Device Name
- SEP3092-01 EUDAMED
- Model / Reference
- SEPLEX EUDAMEDSEP3092-01 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08055348433364 EUDAMED
- Basic UDI-DI
- B-08055348433364 EUDAMED
- EMDN Code
- B06 CELLULAR OR BIOLOGICAL MANIPULATION DEVICES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
Ad Plus by Meika Group S.r.l. — Class I — 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-08055348433364 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Meika Group S.r.l.
- EUDAMED SRN
- IT-MF-000029106
Sources (1)
- EUDAMED 06c77df5-59eb-47e2-b2c9-06b5be19d8d0 61 fields · synced Sep 18, 2026