FTP058

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

  Do not take if you are allergic or hypersensitive to any component. Do not use the product after the expiry date printed on the package. Do not administer to children. The expiry date refers to the product in intact package, properly stored. Even if no side effects are known, it is recommended not to use the product during pregnancy or while breastfeeding. In any case, consult your doctor. In case of concomitant drug therapy, consult your doctor before taking it, as the device may delay or reduce the absorption of drugs administered orally. It is therefore recommended to consult the doctor in case of simultaneous intake of oral medicines which must, in any case, be administered at a distance of at least 2 hours. Consult the doctor if an improvement in clinical status is not noted during the tratment period. Do not use in case the package is not intact. Keep out of reach of children

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

D-FTP058_2KK

Basic UDI-DI

B-FTP058_2KK

Reference / catalog number

FTP058

Issuing entity

EUDAMED

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Lafarmacia. Acidità e Reflusso is a medical device for the treatment of symptoms related to non-specific dyspepsia and gastroesophageal reflux, such as acid regurgitation, retrosternal burning, gastric heartburn.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• G0401ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS