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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 Lozenges HL — Class I MDD by QUIES SAS

MD Atlas
QUIES SAS

EUDAMED last updated this device on Sep 11, 2023

Anti Snoring Lozenges HL

B-03435171521004

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: QUIES SAS
UDI-DI code: 03435171521004
Reference / catalog number: 152100

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Manufacturer information

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

Critical warnings

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

CW010
Keep out of sight and reach of children. The tablet is not suitable for treating sleep apnoea. apnoea. If in doubt about the use of the or if you are pregnant, consult your doctor. your doctor. In case of a serious incident in connection with this device, contact quies@quies.com and inform the competent authority.
CW011
Do not use in case of related respiratory respiratory disease, asthma or allergy to allergy to any of the ingredients. Do not use on injured skin. As with other gums, gastrointestinal gastrointestinal discomfort can be caused by be caused by heavy consumption (bloating, flatulence, laxative effect). Excessive consumption may have laxative effects.
CW032
Do not keep beyond the expiry date.

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 Lozenges HL
UDI-DI code: 03435171521004
Basic UDI-DI: B-03435171521004
Reference / catalog number: 152100
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 Nasal SprayB-03435171561000On 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.