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Angelie EIS

by EMS Handels Gesellschaft m.b.H. EUDAMED

Active European Union

Ref ANG/EIS

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-09120040973193 Basic UDI-DIDate30 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Model / Reference
ANG/EIS
Primary DI / UDI-DI
09120040973193
Basic UDI-DI
B-09120040973193
EMDN Code
N010199 Neurophysiology devices - other
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
AT-MF-000002599

Other devices from EMS Handels Gesellschaft m.b.H.

  • EMS Neurostimulator

    Class IIa

  • Surpass

    Class IIa

  • Surpass LT

    Class IIa

  • Sienna Ultimate

    Class IIa

  • Unique+

    Class IIa

  • Sienna

    Class IIa

Properties

  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No