← Back to catalogue

Nasopharyngeal Airway

EUDAMED

Class I (EU MDR)

Ref NAA95

by Ningbo Luke Medical Devices Co., LTD

Identity

Device Name
Nasopharyngeal Airway EUDAMED
Model / Reference
NAA95 EUDAMED

Identifiers

Primary DI / UDI-DI
06970240893875 EUDAMED
Basic UDI-DI
697024089NAXS EUDAMED
Direct Marketing DI
06970240893875 EUDAMED
EMDN Code
R010101 NASOPHARYNGEAL TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal 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: Nasopharyngeal airway, single-use

Nasopharyngeal Airway by Ningbo Luke Medical Devices Co., LTD — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nasopharyngeal airway, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000011732
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED a88108a9-f9f2-4ca8-b3dd-44f8f9d210de 61 fields · synced Oct 6, 2026