I.V Cannula for Single Use

by Fujian Innpro Medical Technology Co., Ltd. 4 variants

Ref Type I,18G（1.3×32mm)

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697736720LZZ-IV9 Basic UDI-DI 06977367200104UDI-DI	Date23 Sep 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Withdrawn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

Device Name: Sterile I.V Cannula for Single Use
Model / Reference: Type I, 18G（1.3×32mm)

Primary DI / UDI-DI: 06977367200104
Basic UDI-DI: 697736720LZZ-IV9
EMDN Code: C0101010101 Peripheral i.v. catheters, w/o safety systems, with injection valves

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000040556
Authorised representative: Prolinx GmbH DE-AR-000005129

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I.V Cannula for Single Use

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I.V Cannula for Single Use

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Anesthesia Needles for Single Use

Class IIa

See all devices from Fujian Innpro Medical Technology Co., 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