Identity
- Trade Name
- MESOKIT EUDAMED
- Device Name
- Mesoset EUDAMED
- Model / Reference
- MESOSET EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760173232833 EUDAMED
- Basic UDI-DI
- 376017323MESOSETMA EUDAMED
- EMDN Code
- A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Medical Purpose
- The devices in the Mesoset: Mesogreffe consumables set are used to perform a human autologous hair follicle suspension procedure, obtained by mechanical centrifugation of the scalp biopsy, to improve hair density in patients with AGA (androgenetic alopecia). EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Mesokit by Aesthetic Group — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 376017323MESOSETMA | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aesthetic Group
- EUDAMED SRN
- FR-PR-000000348
Sources (1)
- EUDAMED 327cc4bc-6d33-4253-8988-9bb71a028ce8 61 fields · synced Jul 27, 2026