FEGYNO-V12

Organization name

Panin Srl

SRN

IT-MF-000020738

Manufacturer status

Active

6 warnings recorded — scroll inside the panel to see all entries.

• CW009

  EUDAMED did not publish a description for this code.
• CW275

  EUDAMED did not publish a description for this code.
• CW166

  AFTER USE, DISPOSE OF IN ACCORDANCE WITH YOUR NATIONAL LEGISLATION DO NOT DISPERSE IN THE ENVIRONMENT
• CW135

  EUDAMED did not publish a description for this code.
• CW277

  If any symptoms are troublesome or last more than a few days or if you notice any side effects not mentioned, please inform your doctor or pharmacist-(Description) Although FILME GYNO-V is extremely tolerable, in some rare cases it may cause a stinging effect, irritation, allergic or reddening reaction. In these cases discontinue use and consult a doctor. If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
• CW999

  Hypersensitive towards the components.Do not inject nor swallow.

Primary placement in Italy; available across 2 countries total.

Trade name

not provided

UDI-DI code

08033837330165

Basic UDI-DI

B-08033837330165

Reference / catalog number

FEGYNO-V12

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

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.

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

Certificate health across this manufacturer's portfolio.