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Organization name
UDI-DI code
Reference / catalog number

PURESSENTIEL® RESPIRATORY COUGH… — Class IIa MDR

MD Atlas
LABORATOIRE PURESSENTIEL

EUDAMED last updated this device on Apr 28, 2026

PURESSENTIEL® RESPIRATORY COUGH SYRUP

37010568RESPIRATOIREVBMQ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRE PURESSENTIEL
UDI-DI code: 03701056800404
Reference / catalog number: 6095184

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Manufacturer information

Organization name: LABORATOIRE PURESSENTIEL
SRN: BE-MF-000024179
Manufacturer status: Active

Critical warnings

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

CW011
Not recommended for pregnant or breastfeeding women, children under 7 years and people with allergies to hive products. Keep out of the reach of young children. Do not exceed the recommended daily dose. Excessive consumption may have laxative effects. For people receiving medical treatment, seek advice from a healthcare professional.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Oct 21, 2025	Still on market

Device identification

Trade name: PURESSENTIEL® RESPIRATORY COUGH SYRUP
UDI-DI code: 03701056800404
Basic UDI-DI: 37010568RESPIRATOIREVBMQ
Reference / catalog number: 6095184
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Medical device intended to relieve coughs. It acts via its mechanical action to calm coughs that are due to respiratory tracts infections.It: - Clears the upper respiratory tract by hydrating mucus. - Reduces irritation and cough frequency and provides lasting protection for the mucous membranes. - Gives a light refreshing sensation that helps to bear the sting caused by irritation.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q030199NASOPHARYNGEAL 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

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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.