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Armour

by Lars Medicare Pvt Ltd India EUDAMED

Ref 209-1020.22

EMDN C0101010101

Overview

The Armour I.V Cannula is a Class IIa medical device designed for the administration of medications and fluids in various settings, including emergency medicine and intensive care units. Made by mdi Europa GmbH and Lars Medicare Pvt Ltd, this device has undergone rigorous testing to ensure its safety and efficacy.

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08906030751429 Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
209-1020.22
Primary DI / UDI-DI
08906030751429
Basic UDI-DI
B-08906030751429
EMDN Code
C0101010101 Peripheral i.v. catheters, w/o safety systems, with injection valves
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
IN-MF-000025371
Authorised representative
mdi Europa GmbH DE-AR-000006218

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Administering Medicine
Other properties (9)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 13866805-0fb1-4335-bd60-2b920d570eea 61 fields · synced 22 Oct 2026