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WM 23962 (Classic 19)

EUDAMED

Class IIa (EU MDR)

Ref HUE19018KT0019GKModel Classic : tube models consist of different lengths and diameters, different rib Colour, flexibility of cuff and tube

by Plastiflex Group NV

Identity

Trade Name
WM 23962 (Classic 19) EUDAMED
Device Name
Non-heated respiratory tubes EUDAMED
Model / Reference
Classic : tube models consist of different lengths and diameters, different rib Colour, flexibility of cuff and tube EUDAMED
HUE19018KT0019GK EUDAMED

Identifiers

Primary DI / UDI-DI
05404013000319 EUDAMED
Basic UDI-DI
54040130000000000000067 EUDAMED
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

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: Gas-sampling/monitoring respiratory tubing, single-use

WM 23962 (Classic 19) by Plastiflex Group NV — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Plastiflex Group NV
EUDAMED SRN
BE-MF-000008049

Sources (1)

  • EUDAMED d52d1474-a397-4260-8499-7aa4a2698744 61 fields · synced Jun 19, 2026