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ReMeDi

by Neurosynaptic Communications Private Limited EUDAMED

Active European Union

Ref NSCPL/RNK (NSCPL/RN/A, NSCPL/RN/B, NSCPL/RN/C, NSCPL/RN/D)

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08908021482008 Basic UDI-DIDate21 Aug 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  • Withdrawn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

Device Name
ReMeDi® NOVA
Model / Reference
NSCPL/RNK (NSCPL/RN/A, NSCPL/RN/B, NSCPL/RN/C, NSCPL/RN/D)
Primary DI / UDI-DI
08908021482008
Basic UDI-DI
B-08908021482008
EMDN Code
Z1203020202 Transportable/portable multi–parameter patient monitors
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IN-MF-000015562
Authorised representative
Amstermed B.V. NL-AR-000001971

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