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6-MNP 1.5 ToskaniMED EU

by MT.DERM GmbH

Ref EMNPA4806EUMPModel Sterile Accessory N1

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EMTDN1SX Basic UDI-DI +EMTDEMNPA4806EUMP0UDI-DIDate28 Apr 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  • Withdrawn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
6-MNP 1.5 Exceed
Model / Reference
Sterile Accessory N1, EMNPA4806EUMP
Primary DI / UDI-DI
+EMTDEMNPA4806EUMP0
Basic UDI-DI
++EMTDN1SX
EMDN Code
A019013 Percutaneous needles
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

  • Sterile

Other properties (12)

  • 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