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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

PT819 — Class IIa MDR by LABORATOIRES QUINTON…

MD Atlas
LABORATOIRES QUINTON INTERNATIONAL S.L.

EUDAMED last updated this device on Jan 16, 2026

PT819

843700464900137

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRES QUINTON INTERNATIONAL S.L.
UDI-DI code: 08437023259412
Reference / catalog number: PT819

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Manufacturer information

Organization name: LABORATOIRES QUINTON INTERNATIONAL S.L.
SRN: ES-MF-000004083
Manufacturer status: Active

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Critical warnings

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

CW135
EUDAMED did not publish a description for this code.
CW139
EUDAMED did not publish a description for this code.
CW157
EUDAMED did not publish a description for this code.
CW999
The use of this product for other ENT conditions has not been evaluated. Consult your doctor if symptoms persist or are different from those described on the product.Do not use the product if the container is damaged, in case of loss of pressure or if the solution is not released correctly.
CW268
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Nov 27, 2025	Nov 27, 2029
Romania	Nov 27, 2025	Nov 27, 2029

Device identification

Trade name: not provided
UDI-DI code: 08437023259412
Basic UDI-DI: 843700464900137
Reference / catalog number: PT819
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q030103NASAL IRRIGATION SOLUTIONS

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

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.