Skip to content

ToskaniMED

by MT.DERM GmbH

Ref ToskaniMEDModel Microneedling Device MN1

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EMTDMN1HM Basic UDI-DI +EMTDAD64801MP0UDI-DIDate6 Feb 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Exceed
Model / Reference
Microneedling Device MN1, ToskaniMED
Primary DI / UDI-DI
+EMTDAD64801MP0
Basic UDI-DI
++EMTDMN1HM
Direct Marketing DI
+EMTDAD64801MP0
EMDN Code
Z12040203 Dermal regeneration equipment
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
DE-MF-000005784

Other devices from MT.DERM GmbH

See all devices from MT.DERM GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No