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Patient Interfaces(Nasal Cannula)

EUDAMED

Class IIa (EU MDR)

Ref NAModel Hi-NAI-L, Hi-NAI-M, Hi-NAI-S

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Device Name
Patient Interfaces(Nasal Cannula) EUDAMED
Model / Reference
Hi-NAI-L, Hi-NAI-M, Hi-NAI-S EUDAMED
NA EUDAMED

Identifiers

Primary DI / UDI-DI
16975984064526 EUDAMED
Basic UDI-DI
6970341680112301GY EUDAMED
Direct Marketing DI
16975984064526 EUDAMED
EMDN Code
R060280 HUMIDIFICATION SYSTEMS - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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: Tracheostomy tube speech valve

Patient Interfaces(Nasal Cannula) by Shenzhen Lifotronic Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube speech valve.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000005654
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED a3074b2a-cd28-4d05-b374-ea017f49344d 61 fields · synced Jun 18, 2026
  • EUDAMED a3074b2a-cd28-4d05-b374-ea017f49344d-1 61 fields · synced Jun 9, 2026