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Lamed safety

by La-med Healthcare Private (Pvt.) Limited (Ltd.)

Ref IT0133-14Model IV CANNULA WITH SAFETY FEATURE

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8903172SIVC8U Basic UDI-DI 08903172013774UDI-DIDate9 May 2026RegisteredStatusActive

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  • Withdrawn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
IV CANNULA WITH SAFETY FEATURE, IT0133-14
Primary DI / UDI-DI
08903172013774
Basic UDI-DI
8903172SIVC8U
EMDN Code
C0101010201 Peripheral i.v. catheters, with safety systems, with injection valves
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IN-MF-000016008
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from La-med Healthcare Private (Pvt.) Limited (Ltd.)

See all devices from La-med Healthcare Private (Pvt.) Limited (Ltd.) →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No