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Easyflow

by Adria Med S.r.l. 36 variants

Part of a family of 36 devices: see the family page

Ref LF0700Model EASYFLOW

Easyflow (LF0700) is a Class IIb device made by Adria Med S.r.l., registered in EUDAMED on 15 May 2025 (Basic UDI-DI 80522047103EASYKB), active as of 25 Oct 2026.

Active European Union

CE MDR

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80522047103EASYKB Basic UDI-DI 08052204710478UDI-DIDate15 May 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
EASYFLOW, LF0700
Primary DI / UDI-DI
08052204710478
Basic UDI-DI
80522047103EASYKB
Direct marketing DI
08052204710478
EMDN code
A05010101 Elastomeric systems - fixed flow w/o additional bolus
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000020866

Related devices

Category: Elastomeric infusion pump system

Similar devices in this category

Other devices filed under ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS.

Other devices from Adria Med S.r.l.

See all devices from Adria Med S.r.l. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Administering medicine
Other properties (11, all answered No)