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Nasopharyngeal Airway

EUDAMED

Class I (EU MDR)

Ref A06A01501FModel Trumpet

by Well Lead Medical Co., Ltd.

Identity

Trade Name
Nasopharyngeal Airway EUDAMED
Device Name
Nasopharyngeal Airway EUDAMED
Model / Reference
Trumpet EUDAMED
A06A01501F EUDAMED

Identifiers

Primary DI / UDI-DI
06944932774186 EUDAMED
Basic UDI-DI
69449327FA06A01D3 EUDAMED
EMDN Code
R010101 NASOPHARYNGEAL TUBES EUDAMED

Classification

Device Class
Class I 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

Category: Nasopharyngeal airway, single-use

Nasopharyngeal Airway by Well Lead Medical 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

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Manufacturer

EUDAMED SRN
CN-MF-000006728
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 0437b3b4-af22-4e11-ac59-adbb38f7a69c 61 fields · synced Jul 31, 2026