FT.CE.120.3

Organization name

GRUPPO FARMAIMPRESA SRL

SRN

IT-MF-000012625

Manufacturer status

Active

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

• CW999

  Keep out of the reach and sight of children. Do not swallow. Do not use the product if the packaging is not intact. Do not use the product after the expiry date. The expiry date refers to the intact and correctly stored product. Do not use the product in case of vaginal injury or lesions. Do not use in the presence of menstruation. Do not exceed the recommended dose without your doctor's advice. The use, especially if prolonged, can give rise to sensitization phenomena. Where this occurs, stop treatment and consult your doctor in order to establish suitable therapy. It is important to report to the doctor or pharmacist the appearance of undesirable eects not described in this leaflet

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

D-FT.CE.120.3BB

Basic UDI-DI

B-FT.CE.120.3BB

Reference / catalog number

FT.CE.120.3

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

a medical device that helps keep intact the natural defenses of the vagina and facilitates the restoration of the normal vaginal flora. Its particular composition contains Lactic Acid and Fructo-oligosaccharides (FOS) favors, once dissolved in the vagina, the increase in endogenous lactobacilli that in association to the activity on the pH disfavours the action of pathogenic microbiotics such as Streptococci and candida.

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-FT.CE.120.3BB

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

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

• U0803VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS

Certificate health across this manufacturer's portfolio.