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Cathula+

by Hindustan Syringes & Medical Devices Ltd. 112 variants

Ref 03862

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 23 Oct 2026. What this means

Overview

Intravenous Cannula (I V Cannula) - The CATHULA+ Intravenous Cannula is a Class IIa device designed for safe and effective administration of intravenous fluids. It features a sterile single-use design, with a constructed barrier system to prevent endocarditis, and a durable metal body that can withstand rigorous use.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8903347C010101ZM Basic UDI-DI 18903347038622UDI-DIDate8 Oct 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
03862
Primary DI / UDI-DI
18903347038622
Basic UDI-DI
8903347C010101ZM
EMDN Code
C0101010202 Peripheral i.v. catheters, with safety systems, w/o injection valves
Device Class
Class IIa
EU market of registration
Malta

Manufacturer details

EUDAMED SRN
IN-MF-000019164
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Hindustan Syringes & Medical Devices Ltd.

See all devices from Hindustan Syringes & Medical Devices Ltd. →

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