EUDAMED last updated this device on May 29, 2026

NASAL OXYGEN CANNULA

B-06974580753349

On the marketClass IIa

Applicable legislation: —
Organization name: Ningbo Yingmed Medical Instruments Co.,Ltd.
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06974580753349
Reference / catalog number: YM-A1006-2-A

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

NASAL OXYGEN CANNULA is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Ningbo Yingmed Medical Instruments Co.,Ltd.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: NASAL OXYGEN CANNULA
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06974580753349
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-06974580753349
Reference / catalog number: YM-A1006-2-A
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class IIa
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: 1. Attach the oxygen supply tubing to the gas source and set the oxygen to the prescribed flow. 2. Check for gas flow throughout the device. 3. Insert the nasal tips into the nostrils with the two plastic tubes over the ears and under the chin. 4. Gently adjust the plastic slide until the cannula is secure. NOTE: Nasal tips may be trimmed with scissors to fit smaller.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06974580753349

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

R0301020301OXYGEN THERAPY STANDARD NASAL CANNULAS (GOGGLES)

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

Caution
• For single use. Discard after use. • Do not use if package is open or damageded. • Store in cool and dry place. • Ensure that all connections are secure and aircirculates freely through the tubing.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Jan 1, 2023	Still on market

NASAL OXYGEN CANNULA

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Certificates covering this device

Related devices