FT.MDR.26.100

Organization name

GRUPPO FARMAIMPRESA SRL

SRN

IT-MF-000012625

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW999

  The device is not subject to special precautions of use, we note, however: - Do not use the product more than 30 days - The product may appear with two separate phases. After stirring the same should appear as a homogeneous emulsion. - Keep out of reach of children. - Do not exceed recommended dose. - Do not use after the expiration date, the expiry date refers to the product intact and properly stored. - Do not use if package is not intact. - All the components that make up the product including the dropper must be intact. - After a short period of treatment (7 days) with no significant results, consult a doctor - In case of adverse reactions suspend the use of the product and consult your doctor to fix a proper therapy. - During use, if you find the dropper dirty, clean it properly before inserting it into the bottle to prevent possible contamination. - Do not use in cases of suspected intestinal or ileus perforation. Compliance whit the instructions contained in the leaflet reduces the risk of side effects. It is important to inform your doctor or pharmacist about any side effects not listed in this insert leaflet. In case of a serious accident occurring in relation to the medical device report the incident to the Manufacturer and the Competent Authority.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08055748843480

Basic UDI-DI

805574884FTCE16-267U

Reference / catalog number

FT.MDR.26.100

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

RILEFAST CE is a medical device indicated in the treatment in case of: Dyspeptic disorders, gastroenteric meteorism, aerophagia and gas colic in infants, children and adults.

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

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

• G99GASTROINTESTINAL DEVICES - OTHER