Lucovitaal Keelpijn Zuigtabletten NL

Organization name

Labomar S.p.A.

SRN

IT-MF-000007965

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW999

  • The device does not contain sugar, but maltitol and isomalt. If your doctor has diagnosed you with an intolerance with some sugar, contact the doctor before taking this advice. • Keep out of the reach of children. • Do not use in case the package is not intact. • The tablet should not be swallowed, but slowly dissolved in the mouth: do not administer to children under 6 years of age. • If symptoms persist, consult a doctor. • 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. • The expiry date refers to the product in intact package, properly stored.

Primary placement in Netherlands; available across 1 country total.

Trade name

Lucovitaal Keelpijn Zuigtabletten NL

UDI-DI code

D-FTP087_4L7

Basic UDI-DI

B-FTP087_4L7

Reference / catalog number

FTP087

Issuing entity

EUDAMED

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

Lucovitaal Keelpijn Zuigtabletten is a medical device indicated to relieve cough, be it dry, wet, irritative or allergic and for the treatment of irritated throat.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

D-FTP087_4L7

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

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

• V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES