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Klinion

EUDAMED

Class IIa (EU MDR)

Ref C0880365Model PP01 series

by Jiangsu Caina Medical Co., Ltd.

Identity

Trade Name
KLINION EUDAMED
Device Name
Pre-Filled Syringe with Saline EUDAMED
Model / Reference
PP01 series EUDAMED
C0880365 EUDAMED

Identifiers

Primary DI / UDI-DI
06971564462914 EUDAMED
Basic UDI-DI
69715644600340ZU EUDAMED
EMDN Code
A02010701 PREFILLED SYRINGES WITH STERILE PHYSIOLOGICAL SOLUTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

Klinion by Jiangsu Caina Medical Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000011217
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED b5ff0bc7-2207-419c-b39f-47b7142c55fa 61 fields · synced Jun 19, 2026