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Ambix NONCORstick® Safe 20Gx14mm max 21 bar/300 psi-max 4ml/s

EUDAMED

Class IIa (EU MDR)

Ref 8084261

by Fresenius Kabi AG

Identity

Trade Name
Ambix NONCORstick® Safe 20Gx14mm max 21 bar/300 psi-max 4ml/s EUDAMED
Device Name
Cannula Systems EUDAMED
Model / Reference
8084261 EUDAMED

Identifiers

Primary DI / UDI-DI
04250273729382 EUDAMED
Basic UDI-DI
42502737NIV51112a000000WQ EUDAMED
EMDN Code
C01010103 PERIPHERAL I.V. CATHETERS, WITH INTEGRATED EXTENSIONS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Ambix NONCORstick® Safe 20Gx14mm max 21 bar/300 psi-max 4ml/s by Fresenius Kabi AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Fresenius Kabi AG
EUDAMED SRN
DE-MF-000009273

Sources (1)

  • EUDAMED 8f58821e-c791-4f70-9224-3cd872b49ee8 61 fields · synced Jun 18, 2026