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Nasocath Adult

EUDAMED

Class IIa (EU MDR)

Ref 20020Model Nasal Oxygen Catheter/ Cannula

by Poly Medicure Limited

Identity

Trade Name
Nasocath Adult EUDAMED
Device Name
Nasal Oxygen Catheter/ Cannula EUDAMED
Model / Reference
Nasal Oxygen Catheter/ Cannula EUDAMED
20020 EUDAMED

Identifiers

Primary DI / UDI-DI
08902095200209 EUDAMED
Basic UDI-DI
890209520020DF EUDAMED
EMDN Code
R0301020301 OXYGEN THERAPY STANDARD NASAL CANNULAS (GOGGLES) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Nasocath Adult by Poly Medicure Limited — 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

EUDAMED SRN
IN-MF-000043009
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 4097e8f1-58f8-4d99-9702-69a6f998a287 61 fields · synced Jun 18, 2026