Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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_2L5

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_2L5
Reference / catalog number: FTP096

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

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

Related devices

FTP035B-FTP035_1JLOn the market FTP089B-FTP089_1LBOn the market FTPR101805630062FTPR101DKOn the market FTPR101805630062FTPR101DKOn the market FTPR101805630062FTPR101DKOn the market

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)

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

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_2L5
Basic UDI-DI: B-FTP096_2L5
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: NATTERMAN DIRECT VOOR 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_2L5

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

Become a partner of MD Atlas