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Electronic Nasopharyngeal Endoscope

EUDAMED

Class I (EU MDR)

Ref iS-ENC42Model iS-ENF22, iS-ENC32, iS-ENC42, iS-ENF32, iS-ENF42

by Shenzhen Insighters Medical Technology Co., Ltd.

Identity

Trade Name
Electronic Nasopharyngeal Endoscope EUDAMED
Device Name
Electronic Nasopharyngeal Endoscope EUDAMED
Model / Reference
iS-ENF22, iS-ENC32, iS-ENC42, iS-ENF32, iS-ENF42 EUDAMED
iS-ENC42 EUDAMED

Identifiers

Primary DI / UDI-DI
06977800302822 EUDAMED
Basic UDI-DI
697083172ENZK EUDAMED
Direct Marketing DI
06977800302822 EUDAMED
EMDN Code
R010101 NASOPHARYNGEAL TUBES EUDAMED

Classification

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

Electronic Nasopharyngeal Endoscope by Shenzhen Insighters Medical Technology 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-000032018
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 73755582-d076-439f-942f-6796f9a09feb 61 fields · synced Jun 19, 2026