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Stimul 1340

by El.en. SpA

Ref M069A2

Stimul 1340 (M069A2) is a medical device (EU MDR Class IIa; EMDN category neurological stimulators) made by El.en. SpA, registered in EUDAMED on 20 Dec 2021 (Basic UDI-DI 805701776M069XX3K), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805701776M069XX3K Basic UDI-DI 08057017760016UDI-DIDate20 Dec 2021RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
M069A2
Primary DI / UDI-DI
08057017760016
Basic UDI-DI
805701776M069XX3K
EMDN code
Z12101106 Neurological stimulators
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007370

Related devices

Category: Point aesthesiometer

Similar devices in this category

Other devices filed under NEUROLOGICAL STIMULATORS.

Other devices from El.en. SpA

Properties

Other properties (14, all answered No)