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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

FTP096 — Class IIa MDD by Labomar S.p.A.

MD Atlas
Labomar S.p.A.

EUDAMED last updated this device on Apr 20, 2026

FTP096

B-FTP096_1L3

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Labomar S.p.A.
UDI-DI code: D-FTP096_1L3
Reference / catalog number: FTP096

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View device family (Basic UDI)

Manufacturer information

Organization name: Labomar S.p.A.
SRN: IT-MF-000007965
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

CSQ0026240424Supplemented
Quality management systemNotified body: 0373Expiry: Oct 27, 2029

Critical warnings

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

CW999
- Do not take it if you are allergic or hypersensitive to any component. - Do not use the product after the expiry date printed on the package. - Keep out of children's reach. - Shake the stick pack (or bottle) before use. - Wash carefully the measuring cup after use (bottle package only) - Close the bottle accurately after use (bottle package only) - The period of validity after the first opening of the syrup is 3 months (12 weeks) [bottle package only] - Do not use in case the packaging is not intact or damaged; - The syrup has been specifically dosed for children from 3 years old, do not administer to children under 3 years of age. - If you do not notice appreciable results after a short period of treatment (7 days), contact your doctor; in any case do not use for more than 15 days. - So far, no side effects have been observed as a result of the administration of the device. However, if you notice the appearance of side effects, inform your doctor or pharmacist. - The expiry date refers to the packaged product intact, properly stored. - Once the stick pack has been opened, use all its content (stick pack package only)

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-FTP096_1L3
Basic UDI-DI: B-FTP096_1L3
Reference / catalog number: FTP096
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: DAMPO KIDS KINDERSIROOP ALLE HOEST SUIKERVRIJ is a medical device designed for the treatment of dry and wet cough and sore throat.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-FTP096_1L3

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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