Infusion Set for Infusion Pump

by Wenzhou K.L.F. Medical Plastics Co., Ltd 11 variants

Ref 2580213B

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number6944262910B0201TB Basic UDI-DI 06944262912180UDI-DI	Date25 May 2026Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: 2580213B

Primary DI / UDI-DI: 06944262912180
Basic UDI-DI: 6944262910B0201TB
EMDN Code: A03010105 Infusion pump controllers

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000011214
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Wenzhou K.L.F. Medical Plastics Co., Ltd

Extension Set

Class IIa
INFUSION SET (without needle)

Class I
Infusion Set for Infusion Pump

Class IIa
Luer Lock Cap

Class I
TRANSFUSION SET (with needle)

Class IIa
BURETTE INFUSION SET (without needle)

Class I

See all devices from Wenzhou K.L.F. Medical Plastics Co., 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