FTP009

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 applicator (cannula) is disposable. Throw the cannula after use. Do not use in case of allergy to any component; Do not use after the expiry date; Do not use the product if the package is not intact; Store away from light in a cool and dry place; The expiry date refers to the product properly stored in unopened package; Do not swallow; Keep out of the reach of children; Wash your hands before and after use; Do not use in case of ascertained hypersensitivity to any component of the product; Topical use; Compatibility with condoms has not been demonstrated. Use reserved for post-menopausal women.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

D-FTP009_1JK

Basic UDI-DI

B-FTP009_1JK

Reference / catalog number

FTP009

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

GEL VAGINALE ZDP is a medical device for the treatment of vaginal dryness.

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.

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