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I.V. Cannula

by Disposafe Health & Lifecare Limited 10 variants

Ref 3I1

I.V. Cannula (3I1) is a Class IIa device made by Disposafe Health & Lifecare Limited, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-3I1), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-3I1 Basic UDI-DI 3I1UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
IV Cannula with integrated 3 way stopcock with wings and w/o injection port
Model / reference
3I1
Primary DI / UDI-DI
3I1
Basic UDI-DI
B-3I1
EMDN code
C0101010102 Peripheral i.v. catheters, w/o safety systems, w/o injection valves
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
IN-MF-000020265
Authorised representative
AR Experts B.V. NL-AR-000023989

Similar devices in this category

Other devices filed under PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS.

Other devices from Disposafe Health & Lifecare Limited

See all devices from Disposafe Health & Lifecare Limited →

Properties

  • Supplied sterile
Other properties (11, all answered No)