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Mesoset

EUDAMED

Class IIa (EU MDR)

Ref MESOSET

by Aesthetic Group

Identity

Trade Name
MESOSET EUDAMED
Device Name
Mesoset EUDAMED
Model / Reference
MESOSET EUDAMED

Identifiers

Primary DI / UDI-DI
03760173232840 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

Mesoset 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

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Manufacturer

Manufacturer
Aesthetic Group
EUDAMED SRN
FR-PR-000000348

Sources (1)

  • EUDAMED 9ac1d2fd-13ee-4001-b35c-27bb4a5461d7 61 fields · synced Jun 18, 2026