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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Anti Snoring Nasal Spray — Class I MDD by QUIES SAS

MD Atlas
QUIES SAS

EUDAMED last updated this device on Sep 11, 2023

Anti Snoring Nasal Spray

B-03435171561000

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: QUIES SAS
UDI-DI code: 03435171561000
Reference / catalog number: 156100

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Manufacturer information

Organization name: QUIES SAS
SRN: FR-MF-000009589
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
Contains eucalyptus essential oil which may cause skin sensitisation or skin sensitisation or allergic reaction. Keep out of the reach and sight of children. of children. Avoid contact with eyes, Otherwise rinse thoroughly with water. In case of pregnancy, consult your doctor before use. use. In case of doubt with the device talk to your doctor. In the event of a serious incident In case of a serious incident involving this device contact quies@quies.com and inform the relevant authority.
CW011
Do not use in case of irritation. Do not use in case of in case of sleep apnea, related respiratory respiratory disease or asthma. Do not use in case of known allergy to any of the components.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Anti Snoring Nasal Spray
UDI-DI code: 03435171561000
Basic UDI-DI: B-03435171561000
Reference / catalog number: 156100
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q03010299ANTISNORING AND OBSTRUCTIVE SLEEP APNOEA DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

Anti Snoring Lozenges CB-03435171511005On the market Anti Snoring Lozenges HLB-03435171521004On the market Anti Snoring Nasal Strips L343517AS001X9On the market Anti Snoring Nasal Strips SM343517AS001X9On the market Anti Snoring Oral SprayB-03435171531003On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.