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Kit Kath+

by Hindustan Syringes & Medical Devices Ltd. 40 variants

Ref 00194, 04149, 01388, 03790, 03123, 00008, 01888, 05960, 06019, 00750, 00749, 06024, 01442, 02058, 01012, 02443, 03107, 05959, 01395, 02348, 05835, 00758, 02379, 03104, 01444, 01384, 00751, 03181, 00746, 01385, 03113, 03757, 06025, 05830, 00188, 00773, 00012, 01382, 03118, 00681, 01387, 03115, 02631, 02307, 03106, 02317, 06022, 02314, 01922, 01392, 04020

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8903347C010101ZM Basic UDI-DI Date8 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  • Withdrawn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

Trade Name
Kit Kath+
Kitkath+
Kitkath
Device Name
Intravenous Cannula (I V Cannula)
Model / Reference
00194, 04149, 01388, 03790, 03123, 00008, 01888, 05960, 06019, 00750, 00749, 06024, 01442, 02058, 01012, 02443, 03107, 05959, 01395, 02348, 05835, 00758, 02379, 03104, 01444, 01384, 00751, 03181, 00746, 01385, 03113, 03757, 06025, 05830, 00188, 00773, 00012, 01382, 03118, 00681, 01387, 03115, 02631, 02307, 03106, 02317, 06022, 02314, 01922, 01392, 04020
Primary DI / UDI-DI
18903347001947, 18903347041493, 18903347013889, 18903347037908, 18903347031234, 18903347000087, 18903347018884, 18903347059603, 18903347060197, 18903347007505, 18903347007499, 18903347060241, 18903347014428, 18903347020580, 18903347010123, 18903347024434, 18903347031074, 18903347059597, 18903347013957, 18903347023482, 18903347058354, 18903347007581, 18903347023796, 18903347031043, 18903347014442, 18903347013841, 18903347007512, 18903347031814, 18903347007468, 18903347013858, 18903347031135, 18903347037571, 18903347060258, 18903347058309, 18903347001886, 18903347007734, 18903347000124, 18903347013827, 18903347031180, 18903347006812, 18903347013872, 18903347031159, 18903347026315, 18903347023079, 18903347031067, 18903347023178, 18903347060227, 18903347023147, 18903347019225, 18903347013926, 18903347040205
Basic UDI-DI
8903347C010101ZM
Unit of Use DI
08903347060190, 08903347060244, 08903347060251, 08903347060220
Direct Marketing DI
18903347041493
EMDN Code
C0101010101, C0101010102, C0101010201, C0101010202
Device Class
Class IIa
EU market of registration
Malta
Poland

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