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Nasopharyngeal Tube

EUDAMED

Class I (EU MDR)

Ref 061-EOWS-085

by Hangzhou Bever Medical Devices Co., Ltd.

Identity

Trade Name
Nasopharyngeal Tube EUDAMED
Device Name
Nasopharygeal Airway EUDAMED
Model / Reference
061-EOWS-085 EUDAMED

Identifiers

Primary DI / UDI-DI
16948796205807 EUDAMED
Basic UDI-DI
69487962NA0001PE 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

Nasopharyngeal Tube by Hangzhou Bever Medical Devices Co., Ltd. — Class I — 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
CN-MF-000018408
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED c2977330-90d0-4f5b-9c9b-15a4a32d9010 61 fields · synced Jul 12, 2026