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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

17017 — Class IIa MDR by PRANARÔM ESPAÑA S.L.U

MD Atlas
PRANARÔM ESPAÑA S.L.U

EUDAMED last updated this device on Feb 6, 2026

17017

8437023771SYRUPG36M

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRANARÔM ESPAÑA S.L.U
UDI-DI code: 08437023771044
Reference / catalog number: 17017

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Manufacturer information

Organization name: PRANARÔM ESPAÑA S.L.U
SRN: ES-MF-000014215
Manufacturer status: Active

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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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Sep 1, 2022	Still on market
Belgium	Sep 1, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437023771044
Basic UDI-DI: 8437023771SYRUPG36M
Reference / catalog number: 17017
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: Indicated for the treatment of all types of coughs in children from 1 years (>9kg) to 12 years
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 120 MU03

EMDN nomenclature code(s)

V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

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
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Software identification